Publications & Reports

Compartmentalization of innate immune responses in the central nervous system during cryptococcal meningitis/HIV coinfection.

Naranbhai V, Chang CC, Durgiah R, Omarjee S, Lim A, Moosa MY, Elliot JH, Ndung'u T, Lewin SR, French MA, Carr WH
Centre for the AIDS Programme of Research in South Africa - HIV Pathogenesis Programme, Nelson R Mandela School of Medicine, University of KwaZulu Natal, Durban, South Africa cNuffield Department of Medicine, University of Oxford, Oxford, UK dDepartment o

Abstract

OBJECTIVE:: The role of innate immunity in the pathogenesis of cryptococcal meningitis is unclear. We hypothesized that natural killer (NK) cell and monocyte responses show central nervous system (CNS) compartment-specific profiles, and are altered by antifungal therapy and combination antiretroviral therapy (cART) during cryptococcal meningitis/HIV coinfection. DESIGN:: Substudy of a prospective cohort study of adults with cryptococcal meningitis/HIV coinfection in Durban, South Africa. METHODS:: We used multiparametric flow cytometry to study compartmentalization of subsets, CD69 (a marker of activation), CXCR3 and CX3CR1 expression, and cytokine secretion of NK cells and monocytes in freshly collected blood and cerebrospinal fluid (CSF) at diagnosis (n = 23), completion of antifungal therapy induction (n = 19), and after a further 4 weeks of cART (n = 9). RESULTS:: Relative to blood, CSF was enriched with CD56 (immunoregulatory) NK cells (P = 0.0004). At enrolment, CXCR3 expression was more frequent among blood CD56 than either blood CD56 (P <0.0001) or CSF CD56 (P = 0.0002) NK cells. Antifungal therapy diminished blood (P <0.05), but not CSF CXCR3 NK-cell proportions nor CX3CR1 NK-cell proportions. CD56 and CD56 NK cells were more activated in CSF than blood (P <0.0001). Antifungal therapy induction reduced CD56 NK-cell activation in CSF (P = 0.02). Activation of blood CD56 and CD56 NK cells was diminished following cART commencement (P <0.0001, P = 0.03). Immunoregulatory NK cells in CSF tended to secrete higher levels of CXCL10 (P = 0.06) and lower levels of tumor necrosis factor alpha (P = 0.06) than blood immunoregulatory NK cells. CSF was enriched with nonclassical monocytes (P = 0.001), but antifungal therapy restored proportions of classical monocytes (P = 0.007). CONCLUSION:: These results highlight CNS activation, trafficking, and function of NK cells and monocytes in cryptococcal meningitis/HIV and implicate immunoregulatory NK cells and proinflammatory monocytes as potential modulators of cryptococcal meningitis pathogenesis during HIV coinfection.

Full text of this article is available at publisher’s web site at:

http://journals.lww.com/aidsonline/pages/articleviewer.aspx?year=2014&issue=03130&article=00003&type=abstract

Publication

  • Journal: AIDS
  • Published: 21/01/2014
  • Volume: 28
  • Issue: 5
  • Pagination: 657-666

Author

Health Issue