B and T Cell Phenotypic Profiles of African HIV-Infected and HIV-Exposed Uninfected Infants: Associations with Antibody Responses to the Pentavalent Rotavirus Vaccine
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Weinberg, Adriana, et al. B and T Cell Phenotypic Profiles of African Hiv-infected and Hiv-exposed Uninfected Infants: Associations with Antibody Responses to the Pentavalent Rotavirus Vaccine. 2017. https://doi.org/10.17615/szgt-hg94APA
Weinberg, A., Lindsey, J., Bosch, R., Persaud, D., Sato, P., Ogwu, A., Asmelash, A., Bwakura Dangarambezi, M., Chi, B., Canniff, J., Lockman, S., Gaseitsiwe, S., Moyo, S., Smith, C., Moraka, N., & Levin, M. (2017). B and T Cell Phenotypic Profiles of African HIV-Infected and HIV-Exposed Uninfected Infants: Associations with Antibody Responses to the Pentavalent Rotavirus Vaccine. https://doi.org/10.17615/szgt-hg94Chicago
Weinberg, Adriana, Jane Lindsey, Ronald Bosch, Deborah Persaud, Paul Sato, Anthony Ogwu, Aida Asmelash et al. 2017. B and T Cell Phenotypic Profiles of African Hiv-Infected and Hiv-Exposed Uninfected Infants: Associations with Antibody Responses to the Pentavalent Rotavirus Vaccine. https://doi.org/10.17615/szgt-hg94- Creator
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Weinberg, Adriana
- Other Affiliation: Department of Pediatrics; Section of Pediatric Infectious Diseases; University of Colorado Anschutz Medical Campus
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Lindsey, Jane
- Other Affiliation: Center for Biostatistics in AIDS Research; Harvard School of Public Health
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Bosch, Ronald
- Other Affiliation: Center for Biostatistics in AIDS Research; Harvard School of Public Health
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Persaud, Deborah
- Other Affiliation: W. Harry Feinstone Department of Molecular Microbiology and Immunology; Johns Hopkins Bloomberg School of Public Health
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Sato, Paul
- Other Affiliation: Maternal Adolescent and Pediatric Research Branch; NIAID; NIH
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Ogwu, Anthony
- Other Affiliation: Trinity Medical Centre
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Asmelash, Aida
- Other Affiliation: Botswana Harvard AIDS Institute
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Bwakura-Dangarambezi, Mutsa
- Other Affiliation: Department of Paediatrics and Child Health; University of Zimbabwe College of Health Sciences
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Chi, Benjamin H.
- Affiliation: School of Medicine, Department of Obstetrics and Gynecology
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Canniff, Jennifer
- Other Affiliation: Department of Pediatrics; Section of Pediatric Infectious Diseases; University of Colorado Anschutz Medical Campus
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Lockman, Shahin
- Other Affiliation: Department of Pediatrics; Section of Pediatric Infectious Diseases; University of Colorado Anschutz Medical Campus
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Gaseitsiwe, Simani
- Other Affiliation: Department of Pediatrics; Section of Pediatric Infectious Diseases; University of Colorado Anschutz Medical Campus
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Moyo, Sikhulile
- Other Affiliation: Botswana Harvard AIDS Institute Partnership
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Smith, Christiana Elizabeth
- Other Affiliation: Department of Pediatrics; Section of Pediatric Infectious Diseases; University of Colorado Anschutz Medical Campus
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Moraka, Natasha O.
- Other Affiliation: Botswana Harvard AIDS Institute Partnership
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Levin, Myron J.
- Other Affiliation: Department of Pediatrics; Section of Pediatric Infectious Diseases; University of Colorado Anschutz Medical Campus
- Abstract
- We examined associations between B and T cell phenotypic profiles and antibody responses to the pentavalent rotavirus vaccine (RV5) in perinatally HIV-infected (PHIV) infants on antiretroviral therapy and in HIV-exposed uninfected (PHEU) infants enrolled in International Maternal Pediatric Adolescent AIDS Clinical Trials P1072 study ({"type":"clinical-trial","attrs":{"text":"NCT00880698","term_id":"NCT00880698"}}NCT00880698). Of 17 B and T cell subsets analyzed, PHIV and PHEU differed only in the number of CD4+ T cells and frequency of naive B cells, which were higher in PHEU than in PHIV. In contrast, the B and T cell phenotypic profiles of PHIV and PHEU markedly differed from those of geographically matched contemporary HIV-unexposed infants. The frequency of regulatory T and B cells (Treg, Breg) of PHIV and PHEU displayed two patterns of associations: FOXP3+ CD25+ Treg positively correlated with CD4+ T cell numbers; while TGFβ+ Treg and IL10+ Treg and Breg positively correlated with the frequencies of inflammatory and activated T cells. Moreover, the frequencies of activated and inflammatory T cells of PHIV and PHEU positively correlated with the frequency of immature B cells. Correlations were not affected by HIV status and persisted over time. PHIV and PHEU antibody responses to RV5 positively correlated with CD4+ T cell counts and negatively with the proportion of immature B cells, similarly to what has been previously described in chronic HIV infection. Unique to PHIV and PHEU, anti-RV5 antibodies positively correlated with CD4+/CD8+FOXP3+CD25+% and negatively with CD4+IL10+% Tregs. In conclusion, PHEU shared with PHIV abnormal B and T cell phenotypic profiles. PHIV and PHEU antibody responses to RV5 were modulated by typical HIV-associated immune response modifiers except for the association between CD4+/CD8+FOXP3+CD25+Treg and increased antibody production.
- Date of publication
- 2017
- Keyword
- DOI
- Identifier
- Publisher DOI: https://doi.org/10.3389/fimmu.2017.02002
- PMID: 29403482
- PMCID: PMC5780413
- Onescience id: 6421e4b465fea2ffb3c217751ef5674cfaf8e115
- Resource type
- Article
- Rights statement
- In Copyright
- Journal title
- Frontiers in Immunology
- Journal volume
- 8
- Language
- English
- ISSN
- 1664-3224
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