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Volume 287, Issue 1, Pages 79-83 (15 December 2009)


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Cerebrospinal fluid levels of chemokines in HIV infected patients with and without opportunistic infection of the central nervous system

Paulo Pereira Christoab, Márcia de Carvalho Vilelac, Thales Lage Bretasc, Renan Barros Dominguesd, Dirceu Bartolomeu Grecoe, José Antonio Livramentof, Antonio Lucio TeixeiraaceCorresponding Author Informationemail address

Received 9 April 2009; received in revised form 14 August 2009; accepted 3 September 2009. published online 27 September 2009.

Abstract 

Chemokines are chemoattractant cytokines involved in the immune response of a wide variety of diseases. There are few studies assessing their role in opportunistic infections in HIV-infected patients. In this study, we measured CC and CXC chemokines in cerebrospinal fluid (CSF) samples obtained from 40 HIV-infected patients with or without opportunistic infections of the central nervous system (CNS). CSF samples were also analyzed for quantification of total protein, cell count and HIV-1 RNA. HIV+ patients with cryptococcal meningitis had higher levels of CCL2, CCL3, CCL5, CXCL9 and CXCL10 when compared to patients without opportunistic neurological infections. Furthermore, HIV+ patients with associated cryptococcal meningitis had higher levels of CCL3, CXCL9 and CXCL10 when compared to HIV+ patients with associated toxoplasmic encephalitis. CCL3 and CXCL9 levels were positively correlated with CSF HIV-1 RNA levels, CSF protein concentration, and CSF cell count. CXCL10 level was correlated with the CSF viral load and the CSF cell count and CCL5 level was correlated with the CSF cell count. In conclusion, the profile of chemokines in CSF of HIV patients may differ according to the modality of the presented opportunistic infection and according to other biological markers, such as viral load in CSF. These differences are probably related to different patterns of neuroinflammatory responses displayed by patients with different opportunistic neurological infections.

a Neurology Unit, University Hospital, Federal University of Minas Gerais, Belo Horizonte, Brazil

b Eduardo de Menezes Hospital, Belo Horizonte, Brazil

c Group of Neuroimmunology, Laboratory of Immunopharmacology, Institute of Biological Sciences and School of Medicine, Federal University of Minas Gerais, Belo Horizonte, Brazil

d Department of Pathology, Escola Superior de Ciências da Santa Casa de Misericórdia de Vitória (EMESCAM), Brazil

e Department of Internal Medicine, School of Medicine, Federal University of Minas Gerais, Belo Horizonte, Brazil

f Department of Neurology, School of Medicine, University of São Paulo, São Paulo, Brazil

Corresponding Author InformationCorresponding author. Laboratório de Imunofarmacologia, Bloco O4 Sala 202, Departamento de Bioquímica e Imunologia (ICB), Universidade Federal de Minas Gerais, Av. Antonio Carlos, 6627, Pampulha, 31270-901 Belo Horizonte, Brazil. Tel./fax: +55 31 3409 2651.

PII: S0022-510X(09)00844-2

doi:10.1016/j.jns.2009.09.002


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