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      Lactobacillus-Deficient Cervicovaginal Bacterial Communities are Associated with Increased HIV Acquisition in Young South African Women

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          Summary

          Elevated inflammation in the female genital tract is associated with increased HIV risk. Cervicovaginal bacteria modulate genital inflammation, however their role in HIV susceptibility has not been elucidated. In a prospective cohort of young, healthy South African women, we found that individuals with diverse genital bacterial communities dominated by anaerobes other than Gardnerella were at over 4-fold higher risk of acquiring HIV and had increased numbers of activated mucosal CD4 + T cells compared to those with Lactobacillus crispatus-dominant communities. We identified specific bacterial taxa linked with reduced ( L. crispatus) or elevated ( Prevotella, Sneathia, and other anaerobes) inflammation and HIV infection and found that high-risk bacteria increased numbers of activated genital CD4 + T cells in a murine model. Our results suggest that highly prevalent genital bacteria increase HIV risk by inducing mucosal HIV target cells. These findings may be leveraged to reduce HIV acquisition in women living in sub-Saharan Africa.

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          Author and article information

          Journal
          9432918
          8591
          Immunity
          Immunity
          Immunity
          1074-7613
          1097-4180
          5 January 2017
          10 January 2017
          17 January 2017
          17 January 2018
          : 46
          : 1
          : 29-37
          Affiliations
          [1 ]Ragon Institute of MGH, MIT, and Harvard, Massachusetts General Hospital, Cambridge, MA 02139, USA
          [2 ]Harvard Medical School, Boston, MA 02115, USA
          [3 ]Department of Pathology and Immunology, Washington University School of Medicine, Saint Louis, MO 63110, USA
          [4 ]Department of Biostatistics, Harvard School of Public Health, Boston, MA 02115, USA
          [5 ]HIV Pathogenesis Programme, Nelson R. Mandela School of Medicine, University of KwaZulu-Natal, Durban, KwaZulu-Natal, 4001, South Africa
          [6 ]Females Rising through Education, Support, and Health, Durban, KwaZulu-Natal, 4066, South Africa
          [7 ]Department of Medicine, Division of Rheumatology, Immunology and Allergy, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA
          [8 ]Vincent Obstetrics & Gynecology, Massachusetts General Hospital, Boston, MA 02115, USA
          [9 ]Howard Hughes Medical Institute, Chevy Chase, MD 20815, USA
          [10 ]Division of Infectious Diseases, Massachusetts General Hospital, Boston, MA 02115, USA
          [11 ]Institute for Medical Engineering and Science, Massachusetts Institute of Technology, Cambridge, MA 02139, USA
          Author notes
          Corresponding Author and Lead Contact: Dr. Douglas S. Kwon, Ragon Institute of MGH, MIT and Harvard, 400 Technology Square, Cambridge, MA, 02139, USA.; dkwon@ 123456mgh.harvard.edu
          Article
          PMC5270628 PMC5270628 5270628 nihpa840381
          10.1016/j.immuni.2016.12.013
          5270628
          28087240
          eef7edd4-f365-46bc-a202-178832f14a54
          History
          Categories
          Article

          sub-Saharan Africa,HIV acquisition,female genital tract (FGT),vaginal microbiome,mucosal immunology,HIV susceptibility

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