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 IAS 2025, the 13th IAS Conference on HIV Science

Abstract submission

Abstract submissions are now open

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Important dates

20 November 2024
Online abstract submission opens.

22 January 2025, 23:59 Central European Time
Abstract submission closes. Abstracts, as well as amendments to submitted abstracts, will not be accepted after this date (except for late breakers).

8 April 2025
Late-breaker abstract submission opens.

29 April 2025
Late-breaker abstract submission closes.

Scientific tracks

IAS 2025, the 13th IAS Conference on HIV Science, welcomes the submission of abstracts for original contributions to the field in the following scientific tracks:

Track A: Basic science

Track A will explore technological advances and novel insights into HIV persistence, including recent findings for interventions to silence or activate and eliminate HIV. Key topics include gene editing tools, genetically engineered immune cells, and insights from hematopoietic stem cell transplantation. The track will further highlight biomarker research and concepts for engaging innate and adaptive immunity for HIV control. Additionally, novel avenues for prophylactic and therapeutic HIV vaccines will be highlighted, alongside studies on bNAb combinations, bispecific antibodies, cell-based therapies and gene-modified NK cells.

Category

Description

A1

HIV virology

Studies on HIV virology, including viral origins; evolution and diversity; HIV biology; virus-cell interaction; transcription and latency; viral fitness; and persistence and resistance

A2

HIV pathogenesis

Studies on HIV transmission and dissemination; systemic immune activation and inflammation; CD4+ T cell depletion and reconstitution and immune ageing; microbiomes and microbial translocation and correlates of HIV susceptibility; and progression versus control (biomarkers and genetics)

A3

Host immune responses

Studies on innate immunity; humoral immunity and cellular immunity; role of age and biological sex; mucosal immunity; and immune mechanisms of natural control, post-treatment control or post-intervention control

A4

Understanding and targeting persistent HIV reservoirs

Studies on HIV reservoirs and latency; host cellular factors and viral mechanisms of HIV/SIV persistence and latency; identification, characterization and quantification of HIV/SIV reservoirs and rebounding virus; strategies to reduce and/or eliminate viral reservoirs; and strategies to control virologic rebound

A5

Novel treatment and prevention strategies, vaccines and immunotherapies

Studies with preclinical and clinical results from combination strategies to achieve ARV-free control of HIV-1 viremia; gene therapy; immunotherapy (including broadly neutralizing antibodies) and ARVs; small molecules and immunomodulating agents (pharmacodynamics and pharmacokinetics); new approaches to prevent HIV acquisition or treat HIV (new drugs, formulations and/or vehicles); advances in vaccine development; T cell vaccines; novel vectors; adjuvants; and strategies

A6

HIV-associated viruses, co-infections and co-morbidities

Studies with novel insights into the pathophysiology of HIV-1 co-morbidities, in particular in ageing populations; identification of potential therapeutic targets and strategies; and impact of common co-infections (including tuberculosis, viral hepatitis, CMV, HHV-8 and others) on HIV persistence and inflammation

A7

Emerging, re-emerging and neglected virus: epidemiology, pathogenesis, host immune responses, vaccines, immunotherapies and overlap with HIV acquisition

Studies exploring the epidemiology, pathogenesis, host immune responses, vaccines, and therapies of emerging and neglected viral infections, such as arboviruses (Dengue, CHIKV, Zika, Oropuche and others), mpox, SARS-CoV-2, Ebola virus and Marburg; studies on the interaction of these infections with HIV and the concept of “One Health”

Track B: Clinical science

Current one-pill, once-daily regimens and the first all-injectable ART regimens demonstrate continued progress. As people with HIV live longer on ART, co-morbidities remain challenges; these include ageing, cancer, cardiovascular disease, diabetes, neurocognitive disorders, renal and liver impairment, weight gain, frailty and mental health. In addition, co-infections, such as tuberculosis, cryptococcal disease, viral hepatitis and sexually transmitted diseases (including mpox), can cause significant morbidity. Recognizing the clear advances with ART, HIV cure represents an aspirational therapeutic goal, albeit with important ongoing challenges. Additional innovations in ART regimens include long-acting therapies (both oral and injectable), novel ways of administration (implants, patches), and drugs with new mechanisms of action (HIV reverse transcriptase translocation inhibitors, HIV maturation inhibitors, and the development of immunotherapy, such as broadly neutralizing antibodies, or bNAbs). Specific populations face ongoing challenges with ART, including trans individuals, children, pregnant people and people who use drugs. In addition to featuring the latest research findings and controversies regarding ART, Track B will address optimal care and service delivery models and the latest on management of important co-morbidities and co-infections, including ageing and major non-communicable diseases. Finally, Track B will highlight findings and progress from completed and ongoing HIV cure research trials, providing insight on promises, as well as challenges, related to current cure strategies, such as analytical treatment interruption.

Category

Description

B1

Course of HIV disease

Studies that include acute and early infection; impact of co-factors on disease progression; morbidity, mortality and life expectancy in clinical research; and impact of late presentation on clinical and other outcomes

B2

HIV and ageing

Studies on biomarkers, clinical issues related to ageing with HIV, including polypharmacy; frailty (including screening and evidence-based interventions); drug-drug interactions (DDIs); social implications; planning long-term care; and the law related to assisted death

B3

Diagnostic and monitoring tools

Studies with novel insights on assays of immune responses and approaches to assess viral load and ARV resistance/tropism; HIV testing (including self-testing, retesting and point-of-care diagnostics); HIV diagnosis in paediatric and adolescent populations; HIV diagnosis in the context of pre-exposure prophylaxis; viral load and CD4 monitoring; adherence testing; co-infection and co-morbidity diagnostics; simplified and point-of-care safety monitoring (e.g., renal function for people on PrEP and ART); biomarkers for predicting morbidity and mortality; and biomarkers to predict adherence challenges and risk of viral rebound

B4

Co-infections (including opportunistic infections)

Studies on tuberculosis and other opportunistic infections, mpox, viral hepatitis and STIs, including HPV

B5

Co-morbidities and clinical complications of HIV and antiretroviral therapy

Studies of all aspects of co-morbidities and complications of ART, including complications of immune reconstitution, neurologic disorders, mental health, malignancies (HIV- and non-HIV related), cardiovascular disease, bone disease, renal disease, liver disease, diabetes, hypertension, metabolic health (including weight) and other non-communicable diseases and adverse drug reactions; screening (e.g., diabetes) and utility and applicability of primary and secondary prevention strategies; and optimal cohort design to detect HIV and ART impact on co-morbidity risk

B6

Antiretroviral therapies and clinical issues in adults

Studies on ART in acute, first- and second-line therapies; ART in highly treatment-experienced people; regimen simplification and switching; co-formulations of ART and other drugs; pharmacokinetics / pharmacodynamics / pharmacogenomics and therapeutic drug monitoring; drug interactions; long-acting agents and other drug delivery systems (e.g., injectables, implants, dual therapies and microneedle patches); adherence and sex-specific (including cisgender and trans) issues of ART efficacy; adverse reactions and complications; pregnancy (clinical management issues and pharmacokinetics) and contraception; and cost effectiveness of different agents/strategies

B7

Antiretroviral therapies and clinical issues in adolescents and young adults

Studies on clinical issues for adolescents and young adults living with vertically or horizontally acquired HIV; long-acting agents and other drug delivery systems (e.g., injectables, implants, dual therapies and microneedle patches); issues that affect treatment, including adherence, self-disclosure and behavioural health outcomes; mental health and neurocognition; transition of adolescents into adult care; and comprehensive care, including STI treatment and prevention among adolescents and young adults

B8

Antiretroviral therapies and clinical issues in neonates, infants and children

Studies on clinical issues for neonates, infants and children, including pharmacokinetics / pharmacodynamics / pharmacogenomics and therapeutic drug monitoring; drug formulations; long-acting agents and other drug delivery systems (e.g., injectables, implants, dual therapies and microneedle patches); clinical trials; ARV management strategies; cure strategies; adherence; opportunistic infections; TB/HIV co-infection (including treatment and prevention); HIV complications and co-morbidities; HIV-associated co-infections and malignancies in paediatric populations; children exposed to HIV who did not acquire HIV; prevention of vertical HIV transmission; and diagnosis in early infants

B9

Clinical issues specific to key populations

Studies on clinical, legal, social and mental health issues in gay men and other men who have sex with men, racially minoritized communities, sex workers, trans people, people who use drugs, and people in prisons and other closed settings

B10

Cure interventions and other strategies and therapies

Studies on cure interventions; management of analytic treatment interruptions; and nutrition

B11

ART resistance

Studies on all aspects of resistance to ART, including the role of proviral DNA sequencing and next-generation sequencing; the predicted impact of long-acting pre-exposure prophylaxis on transmitted resistance globally; and implications for access to baseline resistance testing

B12

Pandemics, conflict and climate

Studies that include the treatment and prevention of pandemics (including mpox, COVID-19 and influenza); and the impact of conflict and the climate crisis on HIV testing, prevention and care services, including novel models of care and initiatives to mitigate harm

Track C: Epidemiology and prevention science

Track C will discuss newly identified and promising products in development and scale up, such as injectable and implantable long-acting PrEP, combination prevention, use of doxycycline to prevent sexually transmitted infections (STIs), different types and combinations of neutralizing monoclonal antibodies, and innovative HIV testing modalities. A major area of focus will be the scale up and future directions of long-acting injectable PrEP, particularly the scale up of two-monthly intramuscular technologies and challenges preventing its rapid rollout globally, as well as new, cutting-edge science on six-monthly subcutaneous long-acting injectable PrEP from Phase III clinical trials.

Category

Description

C1

Epidemiology of HIV

Studies on the natural history, morbidity patterns and survival of HIV, including all aspects of epidemiology of HIV in specific population groups; factors associated with acquisition, infectivity and transmission of HIV, including the role of syndemics and behaviours and the impact of environmental and political factors; describing HIV transmission through molecular or behavioural epidemiology; analysing HIV incidence and prevalence data across different regions, focusing on key and affected populations, such as men who have sex with men, sex workers, people who inject drugs, and young women; and highlighting epidemiological trends to better understand the dynamics of HIV transmission, identify vulnerable groups, and tailor response strategies accordingly

C2

Surveillance: Measuring the HIV pandemic

Studies on the different approaches to surveillance and behavioural surveillance; measuring and monitoring the impact of HIV, including surveillance among key populations; measuring HIV incidence; measuring the impact of prevention, treatment and/or policy interventions; surveillance of drug resistance; describing transmission with geographical information systems; analysing surveillance data to monitor new acquisitions, HIV-related deaths, and coverage and retention of antiretroviral therapy programmes; integrating treatment coverage data to assess the effectiveness of interventions and ensure continuous access to care for people living with HIV; and using epidemiological data to identify gaps in care and adjust interventions at the community and national levels

C3

Modelling the HIV pandemic

Studies on modelling the HIV pandemic, including models to describe the impact of prevention strategies; modelling the role of social and sexual networks; modelling the impact of syndemics; modelling future healthcare needs and the ability of different service models to meet these needs; mathematical models to simulate the potential impacts of various prevention strategies and anticipate the evolution of the pandemic based on interventions; and cost effectiveness to optimize resource allocation in prevention programmes and guide decision makers toward the most impactful solutions

C4

HIV prevention research

Updates on new antiretroviral drugs, long-acting and on-demand formulations and multi-purpose products used for prevention of HIV; studies on HIV prevention, such as PrEP use and scale up; PEP; voluntary medical male circumcision; condom use, combination prevention strategies; innovative behavioural interventions; structural HIV prevention interventions; measuring and enhancing retention and adherence in HIV prevention programmes; and new vaccines in the pipeline and/or prioritization of these

C5

Integration of HIV services with other services, including sexual and reproductive health services

Studies on integration of services for HIV prevention, sexual and reproductive health and/or hepatitis B/C; optimizing services to provide both PrEP and other STI prevention tools; co-formulation of products for HIV prevention and contraceptive care; point-of-care testing for HIV and other STIs; and development and evaluation of integrated care systems for the management of HIV and other communicable and non-communicable diseases

C6

Population-specific interventions for HIV prevention

Identifying populations not currently reached by prevention programmes; studies on HIV prevention interventions for specific populations, including those targeted at and/or developed by key populations; access to harm reduction interventions; optimizing vertical transmission prevention programmes; studies on PrEP for specific populations, including data on the use of these agents in pregnant and lactating populations, as well as those using hormone therapy; studies that seek inclusion of previously excluded populations in programmes and trials; and efforts to accelerate access to HIV prevention for pregnant and lactating people, adolescents, people who use drugs, and other populations often excluded from programmes

C7

HIV testing

Studies on HIV testing, including demand creation and uptake by different populations; facility-based, community-based, peer-led testing strategies; HIV testing to support prevention; HIV testing to support case finding, re-engagement and/or integration with other services; testing with virtual and/or digital support; HIV self-testing; and HIV testing algorithms

C8

Cascades of HIV prevention, treatment and care

Studies among general population and key population groups (including paediatrics) on strategies to improve HIV linkage to both prevention and treatment, ART initiation, retention in care (first year on ART and beyond) and re-engagement; and population-level studies to monitor health-related quality of life and interventions to optimize this

C9

Monitoring the epidemiology, impact and prevention of new or resurgent pathogens

Studies on all aspects of the epidemiology of new pathogens (e.g., mpox), including among people living with HIV; and effects of new pathogens on HIV epidemiology and prevention, testing and prevention

C10

Monitoring and population-level interventions for non-HIV outcomes

Improving the physical and mental health of people living with HIV; monitoring a range of co-morbidities, including those related to physical and mental health; monitoring progression towards optimal health-related quality of life; and use of surveillance data to monitor non-HIV co-morbidities

C11

Methodology to support epidemiological studies

How to measure incidence; how to detect and monitor recent HIV acquisitions; how to monitor the various stages of the cascade at national and local levels; what new tools and methodological approaches can be used to inform epidemiological studies, including new approaches to data collection and/or new types of data; advances in behavioural surveillance methods; and how new technologies can be used to enhance care without increasing inequalities

Track D: Social and behavioural sciences

Social and behavioural science research continues to guide our understanding of salient, influential factors in the complex dynamics of HIV prevention and care. Mixed methods and adaptive designs offer new insights to identify the tools and resources to most effectively and efficiently design multicomponent intervention packages, differentiated service delivery, expanded care options to provide and support choice, integration of mental health screening and services, and support for economic stability, food security and safety. The guiding theme of Track D will be pushing the boundaries, showcasing research focused on tailoring services through differentiated delivery, choice or other community-centred, local and sustainable approaches. Further areas of focus will include a deep dive into stigma and intersectionality (interventions, critiques of models and innovative thinking in this domain) and the development and implementation of complex multicomponent interventions and strategies to provide whole-person, community-at-the-centre care with special emphasis on groups that are disproportionately impacted by HIV.

Category

Description

D1

Social science theories, frameworks, concepts and methods

Studies that showcase work focused on advancing and reflecting upon social science theories, frameworks, methods and the production of social science knowledge in the HIV field

D2

Social and behavioural aspects and approaches to HIV prevention and living with HIV

Studies that include characterizing the present experience of people living with HIV and populations vulnerable to HIV in specific contexts; intervention approaches to support people with HIV; optimization of use of prevention strategies; status-neutral and U=U interventions; community mobilization and demand creation; harm reduction; and addressing intersectional stigma

D3

Social, cultural, political, legal, environmental and structural determinants of health in different contexts

Studies that highlight new perspectives on social/structural drivers, barriers, resources and contexts that are both external and endogenous/internal to affected communities, including policies and laws

D4

Community-engaged/participatory social science-based interventions

Research specifically engaging communities in innovative participatory methodology ensuring broad community participation and engagement

D5

Key populations and other vulnerable populations: Behavioural, social, cultural, structural and multilevel issues, contexts and interventions

Studies that focus on key populations and other vulnerable populations in specific geographic and cultural contexts, including emerging social vulnerabilities (e.g., increasing migration, the economic crisis and increasing poverty)

D6

Mental health and well-being interventions, programmes and models

Studies that examine innovations in mental health and well-being in HIV care and prevention; integration strategies; tailored measures/screeners; expansion of mental healthcare; and addressing mental health stigma

D7

Gender, sexuality and sexual cultures: Meanings, identities, norms and interventions

Studies that address sexuality; gender issues and gendered relationships; gender-transformative approaches; sexual concurrency; and sexual networks

Track E: Implementation science, economics, systems and synergies

Track E examines the barriers to achieving the 2025 targets and ways to improve our chances of achieving the 2030 targets through both context-specific and standardized approaches of implementation research, econometric study and health systems research to enhance interpretation, transferability and assessment of sustainability. Studies evaluating the barriers to and facilitators of the implementation of existing interventions will be complemented by studies of new strategies for delivery across a range of contexts and a diversity of target groups, from health systems to policy makers to providers to communities to clients. Particular attention will be on studies describing strategies for operationalizing evidence-based interventions and evaluating their sustainability, identifying best-practice methodologies, assessing different stages of implementation, determining key drivers (capacities) needed for change, deploying relevant implementation teams at different levels of the health system, and using measurable quality improvement cycles and policy-practice communication approaches.

Category

Description

E1

Implementation research to scale up HIV testing

Studies that include implementation research focused on preparing for, introducing or evaluating HIV testing strategies. This includes HIV testing and linkage to treatment and prevention; differentiated HIV testing services; innovations in e-health; telehealth and other digital innovations to support HIV testing; novel HIV testing methods; and addressing stigma as a barrier to implementation of HIV testing products and service models

E2

Implementation research to scale up prevention

Studies on the who, what, when, where and why of the HIV prevention toolbox that seek to identify the critical success factors for programme implementation, including acceptability, ease of delivery, cost, vulnerable population and background incidence; supporting HIV prevention effective use and adherence (including oral and long-acting injectable PrEP); prevention of TB and implementation of treatment for latent TB infection; innovations in e-health; and telehealth and other digital innovations to support HIV prevention services, including studies that address stigma as a barrier to implementation of prevention tools and service models

E3

Implementation research to scale up treatment

Studies on the implementation and scale up of HIV treatment, including optimal strategies for delivery of both daily and long-acting ART technologies; care of older people living with HIV; differentiated service delivery across the cascade; strategies to increase retention and re-engagement in HIV services; innovations in e-health; telehealth and other digital innovations to support HIV treatment; access to models of integrated services; enhancing U=U communication; and implementation of viral load monitoring, including studies that address stigma as a barrier to implementation of treatment modalities and service models

E4

Global and national financing, economic evaluation and sustainability

Studies that include national analyses and international assistance; analyses, frameworks and mechanisms for HIV, hepatitis and STI programmes and services and transitional financing; financing HIV within universal health coverage frameworks; payment by results and other performance-based mechanisms; approaches to increasing sustainability, including sustainable financing for civil society; HIV, hepatitis and STI testing and drug access; and approaches and evidence from cross-sectoral programming and financing

E5

Costing, cost effectiveness and affordability

Studies on costing of HIV, hepatitis and STI services; assessments of cost effectiveness (provider and community perspectives); economic evaluation and affordability assessments; and incentives

E6

Health systems, health systems strengthening and partnerships

Studies that include approaches to supporting resilient health systems, community participation and leadership in systems for health, and getting policies into practice; task sharing; public-private partnerships; supporting integration of other health and HIV services; making health systems work for adolescents; services for underserved populations; and effective delivery of long-term chronic care

E7

HIV and development synergies

Studies that focus on combination programming of social drivers of HIV and delivering gender-transformative programmes and tackling sexual and gender-based violence; and studies that showcase new evidence and programmatic lessons on social protection

E8

Integration of HIV services with other health and support services

Studies that move from disease-centric to person-centric approaches and share good practice models of horizontal integration of services for communicable and non-communicable diseases, mental health (including drug and alcohol treatment and harm reduction models), TB and social support

E9

Innovations in data collection, monitoring and evaluation

Studies that include innovations in behavioural data collection and use; innovative approaches to track individuals; innovative uses of data to strengthen systems and programmes; approaches to evaluation of large-scale programmes; approaches to evaluation of combination prevention programmes for monitoring and reporting in the SDG agenda; community-led monitoring; using big data in the HIV response; and approaches to using data to improve programming

Each scientific track is divided into track categories. All abstract authors are asked to choose one scientific track and one track category during the submission process.

By submitting an abstract to the conference, you agree to adhere to the conference embargo policy. The policy specifies that while authors may publish the fact that their abstract has been selected for inclusion in the conference programme, they may NOT share data from the abstract in any form (including print, broadcast or online publication, media release or conference presentation) before its official presentation at IAS 2025.

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Call for abstracts

We encourage work that introduces new ideas, concepts and research and deepens understanding in the field, as well as analyses of both successes and failures. Please read the following guidelines carefully before submitting your abstract:

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  • You can submit your abstracts only online via the conference account on our website. We will not consider submissions by fax, post or email.

  • All abstracts must be written in English.

  • It is your responsibility, as the author, to submit an abstract with the correct wording. Any errors in spelling, grammar or scientific fact in the abstract text will be reproduced exactly as you have typed them. Titles of abstracts selected for presentation will be subject to a spellcheck.

Late-breaker abstracts

We will accept a small number of late-breaker abstracts for oral or poster presentation at IAS 2025.

The late-breaker abstract submission will be open from 8 to 29 April 2025. Late-breaker submissions must introduce data of unquestioned significance that meet a high threshold of scientific merit.

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During abstract submission, authors will have to justify why their abstract should be considered as a late breaker. The same submission rules apply for late-breaker abstracts as for regular abstracts, but each presenting author may present only one late-breaker abstract at the conference.

The percentage of abstracts selected as late breakers will depend on the number of submissions, but selection will be far more rigorous than for regular abstracts.

Questions

  • For technical questions regarding the abstract submission system, please contact the Abstracts team at abstracts@ias2025.org.
  • For general questions regarding abstracts, please see the FAQs.

Policies for abstract submission

Copyright policy

Abstracts must not include libellous or defamatory content. Material presented in abstracts must not violate any copyright laws. If figures, graphics and/or images have been taken from sources not copyrighted by the author, it is the author’s sole responsibility to secure the rights from the copyright holder in writing to reproduce those figures, graphics and/or images for both worldwide print and web publication. The author must bear all reproduction costs charged by the copyright holder.

Language

As the official IAS 2025 language is English, all abstracts must be in English. If English is not your native language, please arrange for a native English speaker to review your abstract before submission. Please use the UNAIDS terminology guidelines and People First terminology when drafting and submitting your abstract. Please ensure that you DO NOT use stigmatizing language. DO use: people or person living with HIV; person or people with TB; people or person living with HIV and TB; healthcare seekers or clients. DO NOT label people as: HIV-infected; infected; co-infected; cases; carriers; victims; patients.

Resubmission policy

An abstract that has been previously published or presented at a national, regional or international meeting can be submitted to IAS 2025 only if there are new methods, findings, updated information or other valid reasons for resubmitting.

If preliminary or partial data have been published or presented previously, the submitting author will be required to provide details of the publication or presentation, along with a justification of why the abstract merits being considered for IAS 2025. The IAS 2025 Organizing Committee will consider this information when making final decisions.

If the author neglects to provide these required details and justification or if evidence of previous publication or presentation is found, the abstract will be rejected.

Plagiarism

The conference organizers regard plagiarism as serious professional misconduct. All abstracts are screened for plagiarism and, when identified, the abstract and any other abstracts submitted by the same author are rejected. In addition, the submitting author’s account and scholarship application (if one has been submitted) will be cancelled.

Ethical research declaration

The conference supports only research that has been conducted according to the protocol approved by the institutional or local committee on ethics in human investigation. Where no such committee exists, the research should have been conducted in accordance with the principles of the Declaration of Helsinki of the World Medical Association. If you answer “no” or “not applicable”, you will be required to provide a written explanation for your answer. The IAS 2025 Organizing Committee may inquire further into ethical aspects when evaluating abstracts.

Artificial Intelligence

The use of generative Artificial Intelligence tools to develop any portion of an abstract must be disclosed and described in detail in the Methods section. The author is fully responsible for the accuracy of any information provided in the abstract, including the portions developed by the generative Artificial Intelligence tools. The use of tools to improve language quality is not to be considered generative Artificial Intelligence and does not need to be disclosed. The decision about whether the use of generative Artificial Intelligence tools is acceptable in a submitted abstract lies with the IAS 2025 Organizing Committee. 

Conference embargo policy

As is the case with most scientific and medical conferences, abstracts from IAS 2025 are released to delegates and media under a strict embargo policy. You can find the conference embargo policy here. All conference delegates, presenters and media agree to respect this policy.

Abstract submission process

Conference account

Authors must create a conference account to submit an abstract. More than one abstract can be submitted through a conference account. After an abstract has been created, modifications can be made until 22 January 2025, 23:59 Central European Time.

Choosing a track category

The track category is the general heading under which the abstract will be reviewed and later published in the conference materials if accepted. During the submission process, you will be asked to select one track category for your abstract. Choose the track category that best describes the subject of the abstract.

Abstract structure

The conference offers two options for abstract submission:

Option 1

This is suitable for research conducted in all disciplines. Abstracts submitted under Option 1 should contain concise statements of:

  • Background: Indicate the purpose and objective of the research, the hypothesis that was tested, or a description of the problem being analysed or evaluated.
  • Methods: Describe the study period, setting and location, study design, study population, data collection and methods of analysis used.
  • Results: Present as clearly and in as much detail as possible the findings and/or outcomes of the study. Please disaggregate data by age and gender where possible and summarize any specific results.
  • Conclusions: Explain the significance of your study’s findings and/or outcomes for HIV prevention, treatment, care and/or support and future implications of the results.

The following review criteria will be used in scoring abstracts submitted under Option 1:

  1. Impact: Does the study contribute meaningfully to the field as an original study or a useful confirmatory study?  
  1. Science: Is the study/research design of high quality and sufficiently explained, including clearly stated questions, data sources, data collection procedures and appropriate analytic/methodological approach and with clear and consistent results? 

Option 2

This is suitable for lessons learnt through programme, project or policy implementation or management. Abstracts submitted under Option 2 should contain concise statements of:

  • Background: Summarize the purpose, scope and objectives of the programme, project or policy.
  • Description: Describe the programme, project or policy period, setting and location, structure, key population (if applicable) and activities and interventions undertaken in support of the programme, project or policy.
  • Lessons learnt: Present as clearly and in as much detail as possible the findings and/or outcomes of the programme, project or policy. Include an analysis or evaluation of lessons learnt and best practices. Please summarize any specific results that support your lessons learnt and best practices.
  • Conclusions/next steps: Explain the significance of the findings and/or outcomes of the programme, project or policy for HIV prevention, treatment, care and/or support and future implications of the results.

The following review criteria will apply to abstracts submitted under Option 2:

  1. Impact: Does the study contribute meaningfully to the field as an original study or a useful confirmatory study? 
  1. Science: Is the programme, project or policy implementation of high quality and sufficiently explained, including justified objective, detailed findings/outcomes, data sources and feasibility and with clear and consistent results?  

Disaggregation by sex and other demographic data in abstracts 

Authors are encouraged to provide a breakdown of data by gender identity and/or assigned sex at birth and other demographics, such as age, geographic region, racial/ethnic identity and/or other relevant demographic characteristics in submitted abstracts when appropriate. Your abstract should include the number and percentage of men and women who participated in your research or project (and additional breakdown by gender, age and/or ethnicity if appropriate). Results should be disaggregated by sex/gender and other relevant demographics. Analyses of any gender-based differences or any other differences between sub-populations should be provided in the Results or Lessons learnt sections if relevant.

Meaningful engagement of people living with HIV in research 

The IAS actively encourages the submission of research that meaningfully engages and involves people living with HIV, fostering collaboration through co-authorship and presenting author roles, in alignment with the principles outlined in the UNAIDS Global Advocacy Policy Brief on the Greater Involvement of People Living with HIV (GIPA).

Font

Use a standard font, such as Arial, when formatting the text. This helps prevent special characters from getting lost when copying the text to the online abstract submission form. Ensure that you check the final abstract with the system’s preview function before submission, and edit or replace if necessary.

Word limits

The abstract is limited to 350 words. Titles are limited to 30 words.

A maximum of two tables and/or graphs or images can be included. A graph or image (in JPG, GIF or PNG, ideally 600dpi) counts as 50 words and a table counts as five words per row (50 words maximum).

Common reasons for abstract rejection:

  • Abstract poorly written
  • Not enough new information
  • Clear objective and/or hypothesis missing
  • Methods (either quantitative or qualitative) inadequate and/or insufficient to support conclusions
  • Summary of essential results inadequate and/or missing
  • Study conclusions not supported by the data
  • Linkage between different parts of the abstract not comprehensible
  • Duplicate or overlap with another abstract
  • Study too preliminary or insufficient to draw conclusions
  • Study originality lacking

Recommendations:

  • Abstracts should disclose primary findings and avoid, whenever possible, promissory statements, such as “experiments are in progress” or “results/lessons learnt will be discussed”.
  • If English is not your native language, arrange for a native English speaker to review your abstract before submission.

Submission confirmation

After submission of the abstract, a confirmation email will be sent to the abstract submitter. To receive confirmation, please ensure that your email provider does not mark emails from ias2025@abstractserver.com as spam. 

Support programmes

The IAS established the Abstract Mentor Programme (AMP) at AIDS 2004, the 15th International AIDS Conference. For two decades, the AMP has lifted the chances of abstracts of mentees, particularly from resource-limited settings, being accepted for presentation. Building on this, the IAS remains determined to assist less-experienced and early-career researchers in improving their abstract submissions through innovative mentorship and learning initiatives. We invite you to join the IAS Mentorship Programme, register for the upcoming JIAS workshop on abstract writing, and visit the IAS+ learning platform.

Scholarships

Abstract presenters interested in applying for a scholarship must submit their application by 22 January 2025. Please visit the Scholarship page for more information.

Abstract review and selection process

Abstract review

All submitted abstracts will go through a blind peer-review process carried out by international reviewers. At least three reviewers will review each abstract.

Abstract selection

A small number of abstracts will be selected for oral presentation. The majority of abstracts selected for the conference will be displayed as paper posters on site.

Notification of acceptance or rejection to the corresponding author

Notification of acceptance or rejection will be sent to the submitting (corresponding) author by mid-April. Please note that only the corresponding author will receive an email concerning the abstract; this author is responsible for informing all co-authors of the status of the abstract. The presenting author, whose abstract has been accepted, will receive instructions for the presentation of their abstract.

Rule of two

Each presenting author may present a maximum of two abstracts at the conference. The number of submissions is, however, not limited. If an author has more than two abstracts accepted for presentation, a co-author must be named as the presenting author for one or more abstracts.

Each presenting author may also present one late-breaker abstract at the conference.

Publication of accepted abstracts

The submission of an abstract constitutes the author(s)’ consent for publication. If the abstract is accepted, the author(s) agree that the abstract is published under the Creative Commons Attribution 3.0 Unported (CC BY 3.0) licence. The licence allows third parties to share the published work (copy, distribute, transmit) and to adapt it for any purposes, under the condition that IAS 2025 and authors are given credit and that in the event of reuse or distribution, the terms of this licence are made clear. Authors retain the copyright of their abstract, with first publication rights granted to the IAS.

Accepted abstracts may, therefore, be published on IAS websites and in such publications as the IAS 2025 online conference programme and other conference materials, the IAS abstract archive and the Journal of the International AIDS Society (JIAS).

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Co-submission

Abstract submitters

The IAS has approved several conferences for abstract co-submission leading up to IAS 2025. This means that you will be able to submit your abstract to the selected conferences, listed below, and to IAS 2025 without breaking our embargo policy. Co-submission does not apply to IAS 2025 late-breaker abstracts. Conference organizers have until 31 March 2025 to request co-submission.

Once conferences/events have been approved for co-submission they will be listed below.

The approved co-submission conferences so far are:

Conference or workshop organizers

If you are inviting authors to present abstracts at your conference or workshop in the run up to IAS 2025, you may wish to consider applying for abstract co-submission with IAS 2025. Co-submission means that selected abstracts may be presented at your event and at IAS 2025 without breaking the embargo policy even though your event will take place before the conference.

To apply for co-submission of abstracts with IAS 2025, your event should meet the following conditions:

  • The event must be closed.

    • Delegates will attend the event on an invite-only or paid-registration basis (that is, sessions are not open to the general public).

    • Media representatives are not invited or they must agree to comply with the IAS 2025 embargo policy.

    • Any sessions involving co-submitted abstracts that will be recorded must comply with the IAS 2025 embargo policy.

  • A final list of abstracts presented at the event must be shared with the IAS before the event.

  • Authors must submit their abstract using the IAS 2025 submission system if they wish to be considered for inclusion in IAS 2025.

In addition, although not mandatory, for events that meet the conditions, it is highly recommended that organizers apply for IAS 2025 Affiliated Independent Event status.

If you wish to apply for co-submission for your conference or workshop, please contact us at abstracts@ias2025.org. The deadline to apply for co-submission is 31 March 2025.

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FAQs

What is an abstract?

For IAS 2025, the 13th IAS Conference on HIV Science, an abstract is a standalone statement that briefly explains the essential information of a study, research project, policy or programme.

Where can I read more about the scientific tracks?

You can find detailed descriptions of the scope and objectives of each scientific track, as defined by the IAS 2025 Organizing Committee, on the abstract submission page.

When is the submission deadline for abstracts?

The deadline for submission of abstracts is 22 January 2025, 23:59 Central European Time.

My project is ongoing and there are no results yet. Should I submit an abstract?

Abstracts are intended to present scientific studies, research, programmes and policies, highlighting the methods and/or description and results and/or recommendations. If you are describing a study that is still in the planning stage, it would not be suitable for submission unless the methods that you use are, for example, of particular scientific interest. However, if your study is ongoing and you have preliminary data that seem relevant or significant, please submit an abstract.

What is a late-breaker abstract?

Late-breaker submissions must introduce data of unquestioned significance. Data analysed after the regular submission deadline (22 January 2025) should not be sent in for late breakers if the data do not meet an extremely high standard of scientific merit. The percentage of abstracts selected as late breakers will depend on the number of submissions made, but selection will certainly be more rigorous than for regular abstracts. A small number of late-breaker abstracts will be accepted for presentation orally or as posters at the conference.

During their abstract submission, authors will have to declare the reason why their abstract is a late breaker. The same submission rules apply for late-breaker abstracts as for regular abstracts, but each presenting author may present only one late-breaker abstract at the conference. Late-breaker abstract submission will be open from 8 to 29 April 2025.

What is the required structure for an abstract?

An abstract consists of a title, author list and abstract text no longer than 350 words. It can also include tables, graphs and/or images. Literature references should not be included.

IAS 2025 offers two options for abstract submission:

Option 1

This is suitable for research conducted in all disciplines. Abstracts submitted under Option 1 should contain concise statements of:

  • Background: Indicate the purpose and objective of the research, the hypothesis that was tested or a description of the problem being analysed or evaluated.
  • Methods: Describe the study period, setting and location, study design, study population, data collection and methods of analysis used.
  • Results: Present as clearly and in as much detail as possible the findings and/or outcomes of the study. Please disaggregate data by age and gender where possible and summarize any specific results.
  • Conclusions: Explain the significance of the findings and/or outcomes of your study for HIV prevention, treatment, care and/or support and future implications of the results.

Option 2

This is suitable for lessons learnt through programme, project or policy implementation or management. Abstracts submitted under Option 2 should contain concise statements of:

  • Background: Summarize the purpose, scope and objectives of the programme, project or policy.
  • Description: Describe the programme, project or policy period, setting and location, structure, key population (if applicable) and activities and interventions undertaken in support of the programme, project or policy.
  • Lessons learnt: Present as clearly and in as much detail as possible the findings and/or outcomes of the programme, project or policy. Include an analysis or evaluation of lessons learnt and best practices. Please summarize any specific results that support your lessons learnt and best practices.
  • Conclusions/next steps: Explain the significance of the findings and/or outcomes of the programme, project or policy for HIV prevention, treatment, care and/or support and future implications of the results.

How do I submit an abstract?

Before submitting an abstract, you will be asked to create a conference account. One or several abstracts can be submitted through this account.

To submit abstracts, please log in to your conference account and click on the “Abstract submission” box on the conference account overview page. Then click on the red button, “Submit an abstract”. In the abstract submission system:

  1. Select the track, category and country of research. Enter your abstract title and text.
  2. Enter the presenting author and co-authors (individually).
  3. Preview your abstract and check format and correctness.
  4. Submit your abstract.

After an abstract has been created, modifications can be made at any time until the submission deadline. After submission, the abstract submitter will receive a confirmation email with an abstract reference number. Please refer to this reference number in all conference correspondence.

Once submitted, can I still modify my abstract?

After an abstract has been submitted via the conference account, modifications can be made until the submission deadline, 22 January 2025. After making your modifications, you need to resubmit your abstract. No modifications will be accepted after 22 January 2025.

How should I write the title of my abstract?

A good abstract title is short, specific, representative and informative. It helps the reviewers categorize your abstract and, if accepted, it may help conference delegates find your presentation. The title should summarize your abstract without going into excessive details. Describe the topic clearly, including, for example, the population, country and issue of the research. Titles are limited to 30 words.

Can I include a table, graph or image in my abstract?

It is permitted but not mandatory to include tables, graphs and/or images in the abstract. A maximum of two tables, graphs or images in total can be included. A graph or image (in JPG, GIF or PNG, ideally 600dpi) counts as 50 words, and a table counts as five words per row (50 words maximum). As a reminder, the abstract text body is limited to 350 words.

Please create your table or upload your graph or image following the instructions in the abstract submission system. Place the table, graph or image into your abstract text and save the changes. Review the abstract preview page to ensure that your table, graph and/or image displays properly.

How many co-authors can I include?

There is no limit to the number of co-authors per abstract, although we strongly recommend the use of a study group name for abstracts with a high number of co-authors. A person can be listed as a co-author if they meet ALL the following criteria:

  1. They made substantial contributions to concept and design, acquisition of data or analysis and interpretation of data.
  2. They drafted the abstract or revised it for intellectual content.
  3. They approved the final version to be submitted.

Do I need to disclose information about any conflict of interest in my abstract?

If the abstract is accepted, the presenting authors are asked to disclose all financial and personal relationships between themselves and others that might be perceived as biasing their work. The IAS asks that all presenting authors disclose any conflicts of interest at the time of presentation for the benefit of conference delegates. The purpose of this is to guarantee that all potential conflicts of interest are recognized and that mechanisms to resolve them before the conference are implemented.

Material presented in abstracts should not violate any copyright laws. If figures, graphics and/or images have been taken from sources not copyrighted by the author, it is the author’s sole responsibility to secure the rights from the copyright holder in writing to reproduce those figures, graphics and/or images for both worldwide print and web publication. The author must bear all reproduction costs charged by the copyright holder.

Who selects the abstracts and decides how they will be presented?

All submitted abstracts will go through a blind peer-review process by international reviewers. At least three reviewers will review each abstract. The IAS 2025 Organizing Committee makes the final selection of abstracts to be included in the conference programme.

A small number of abstracts will be selected for oral presentation. The majority of abstracts selected for the conference will be presented as paper posters on site.

How can I increase the chances of my abstract being accepted?

The methodology or study design presented in your abstract should be appropriate to address the purpose and objectives. Results or lessons learnt should be clearly presented and support the conclusions. In addition, the findings should contribute to the advancement of knowledge and development in the field.

If English is not your native language, we strongly recommend that you arrange for a native English speaker working in your field to review your abstract before submission.

Please use the UNAIDS terminology guidelines and People First terminology when drafting and submitting your abstract. Please ensure that you DO NOT use stigmatizing language. DO use: people or person living with HIV; person or people with TB; person or people living with HIV and TB; healthcare seekers or clients. DO NOT label people as: HIV-infected; infected; co-infected; cases; carriers; victims; patients.

You may check the common reasons for abstract rejection in the abstract submission guidelines found further up on this page.

You may also review examples of abstracts from previous conferences.

The IAS remains determined to assist less-experienced and early-career researchers in improving their abstract submissions through innovative mentorship and learning initiatives. We invite you to join the IAS Mentorship Programme, register for the upcoming JIAS interactive workshops, and visit the IAS+ learning platform.

When will I be notified if my abstract submission has been successful?

Notification of acceptance or rejection will be sent to the submitting (corresponding) author by early April.

I need a certificate that shows that my abstract was accepted for the conference. Who do I contact?

To obtain a certificate for abstracts accepted, please contact abstracts@ias2025.org.

Who has the copyright for my abstract after submission?

The submission of the abstract constitutes the authors’ consent to publish. If the abstract is accepted, the authors agree that their abstract can be published under the Creative Commons Attribution 3.0 Unported (CC BY 3.0) licence. The licence allows third parties to share the published work (copy, distribute, transmit) and adapt it for any purposes, on condition that IAS 2025 and the authors are given credit and that in the event of reuse or distribution, the terms of this licence are made clear. Authors retain the copyright of their abstracts, with first publication rights granted to the IAS.

Will there be an abstract book for IAS 2025?

An electronic abstract book will be available immediately after the conference free of charge on the conference website.

Where will my abstract be published?

Accepted abstracts will be published on IAS websites and in such publications as the IAS 2025 online programme and other conference materials and the IAS abstract archive. Oral abstracts will be published in the Journal of the International AIDS Society (JIAS).

The IAS promotes the use of non-stigmatizing, people-first language. The translations are all automated in the interest of making our content as widely accessible as possible. Regretfully, they may not always adhere to the people-first language of the original version.