4.7 Article

Cryptococcus neoformans Ex Vivo Capsule Size Is Associated With Intracranial Pressure and Host Immune Response in HIV-associated Cryptococcal Meningitis

期刊

JOURNAL OF INFECTIOUS DISEASES
卷 209, 期 1, 页码 74-82

出版社

OXFORD UNIV PRESS INC
DOI: 10.1093/infdis/jit435

关键词

Cryptococcus neoformans; cryptococcal meningitis; HIV; polysaccharide capsule; intracranial pressure; immune response; CSF; human

资金

  1. Wellcome Trust Intermediate Fellowship [WT 089966]
  2. US National Institutes of Health [U01A1089244, R21NS065713, K23A1073192]
  3. Royal Academy of Engineering
  4. EPSRC
  5. EPSRC
  6. Center for AIDS Research at the Albert Einstein College of Medicine and Montefiore Medical Center [NIH AI-51519]
  7. [P.21 41087564]
  8. [RO1 A1059681]
  9. NATIONAL INSTITUTE OF ALLERGY AND INFECTIOUS DISEASES [P30AI051519, K23AI073192, U01AI089244, R01AI059681] Funding Source: NIH RePORTER
  10. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R21NS065713] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Background. The Cryptococcus neoformans polysaccharide capsule is a well-characterized virulence factor with immunomodulatory properties. The organism and/or shed capsule is postulated to raise intracranial pressure (ICP) in cryptococcal meningitis (CM) by mechanical obstruction of cerebrospinal fluid (CSF) outflow. Little is known regarding capsule phenotype in human cryptococcosis. We investigated the relationship of ex vivo CSF capsular phenotype with ICP and CSF immune response, as well as in vitro phenotype. Methods. In total, 134 human immunodeficiency virus HIM-infected Ugandan adults with CM had serial lumbar punctures with measurement of CSF opening pressures, quantitative cultures, ex vivo capsule size and shedding, viscosity, and CSF cytokines; 108 had complete data. Induced capsular size and shedding were measured in vitro for 48 C. neoformans isolates. Results. Cryptococcal strains producing larger ex vivo capsules in the baseline (pretreatment) CSF correlated with higher ICP (P =.02), slower rate of fungal clearance (P =.02), and paucity of CSF inflammation, including decreased CSF white blood cell (WBC) count (P <.001), interleukin (IL)-4 (P =.02), IL-6 (P =.01), IL-7 (P =.04), IL-8 (P=.03), and interferon 7 (P=.03). CSF capsule shedding did not correlate with ICP. On multivariable analysis, capsule size remained independently associated with ICP. Ex vivo capsular size and shedding did not correlate with that of the same isolates grown in vitro. Conclusions. Cryptococcal capsule size ex vivo is an important contributor to virulence in human cryptococcal meningitis.

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