4.8 Article

Dysregulated Humoral Immunity to Nontyphoidal Salmonella in HIV-Infected African Adults

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SCIENCE
卷 328, 期 5977, 页码 508-512

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AMER ASSOC ADVANCEMENT SCIENCE
DOI: 10.1126/science.1180346

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资金

  1. GlaxoSmithKline
  2. Wellcome Trust
  3. University of Birmingham
  4. Medical Research Council, UK
  5. UK Biotechnology and Biological Sciences Research Council, UK
  6. National Institute for Health Research Cambridge Biomedical Research Center
  7. National Council for Science and Technology (CONACyT) Mexico [SALUD-2007-C01-69779]
  8. Biotechnology and Biological Sciences Research Council [BB/F022778/1] Funding Source: researchfish
  9. Medical Research Council [G108/574, G0701275, G9818340, G8402371, G9818340B] Funding Source: researchfish
  10. BBSRC [BB/F022778/1] Funding Source: UKRI
  11. MRC [G9818340, G108/574, G8402371, G0701275] Funding Source: UKRI

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Nontyphoidal Salmonellae are a major cause of life-threatening bacteremia among HIV-infected individuals. Although cell-mediated immunity controls intracellular infection, antibodies protect against Salmonella bacteremia. We report that high-titer antibodies specific for Salmonella lipopolysaccharide (LPS) are associated with a lack of Salmonella-killing in HIV-infected African adults. Killing was restored by genetically shortening LPS from the target Salmonella or removing LPS-specific antibodies from serum. Complement-mediated killing of Salmonella by healthy serum is shown to be induced specifically by antibodies against outer membrane proteins. This killing is lost when excess antibody against Salmonella LPS is added. Thus, our study indicates that impaired immunity against nontyphoidal Salmonella bacteremia in HIV infection results from excess inhibitory antibodies against Salmonella LPS, whereas serum killing of Salmonella is induced by antibodies against outer membrane proteins.

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