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Updated: Mar 12, 2026

An In Vitro Model for Measuring Immune Responses to Malaria in the Context of HIV Co-infection
Published on: October 6, 2015
Trained Immunity and Susceptibility to HIV
1Center for Biologics Evaluation and Research, U.S. Food and Drug Administration, Silver Spring, Maryland, USA steven.derrick@fda.hhs.gov.
A novel Mycobacterium tuberculosis-simian immunodeficiency virus vaccine (AMTB-SIV) may increase susceptibility to simian immunodeficiency virus (SIV) infection in infant macaques. This effect might be linked to trained immunity and enhanced CD4+ T cell responses.
Area of Science:
- Immunology
- Vaccinology
- Infectious Diseases
Background:
- A dual-purpose attenuated Mycobacterium tuberculosis-simian immunodeficiency virus vaccine (AMTB-SIV) was developed.
- Previous research on vaccine-induced trained immunity has shown varied effects on subsequent pathogen challenge.
Purpose of the Study:
- To investigate the impact of the AMTB-SIV vaccine on susceptibility to simian immunodeficiency virus (SIV) infection in infant macaques.
- To explore the potential role of trained immunity and CD4+ T cell activation in vaccine-induced SIV susceptibility.
Main Methods:
- Infant macaques were immunized with the AMTB-SIV vaccine.
- Immunized and non-immunized macaques were subsequently exposed orally to SIV.
- CD4+ T cell responses and susceptibility to infection were monitored.
Main Results:
- Infant macaques immunized with AMTB-SIV required fewer oral SIV exposures to become infected compared to non-immunized controls.
- The study suggests a potential link between vaccine-induced trained immunity and augmented CD4+ T cell activation.
- This activation may lead to increased susceptibility to SIV infection.
Conclusions:
- The AMTB-SIV vaccine may inadvertently enhance susceptibility to SIV infection in infant macaques.
- Trained immunity and CD4+ T cell responses could play a critical role in this phenomenon.
- Further research is needed to understand the implications for human immunodeficiency virus (HIV) vaccine development.
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