High levels of T lymphocyte activation in Leishmania-HIV-1 co-infected individuals despite low HIV viral load


Autoria(s): SANTOS-OLIVEIRA, Joanna R.; GIACOIA-GRIPP, Carmem B. W.; OLIVEIRA, Priscilla Alexandrino de; AMATO, Valdir S.; LINDOSO, Jose Angelo L.; Goto, Hiro; OLIVEIRA-NETO, Manoel P.; MATTOS, Marise S.; GRINSZTEJN, Beatriz; MORGADO, Mariza G.; CRUZ, Alda M. da
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

18/04/2012

18/04/2012

2010

Resumo

Background: Concomitant infections may influence HIV progression by causing chronic activation leading to decline in T-cell function. In the Americas, visceral (AVL) and tegumentary leishmaniasis (ATL) have emerged as important opportunistic infections in HIV-AIDS patients and both of those diseases have been implicated as potentially important co-factors in disease progression. We investigated whether leishmaniasis increases lymphocyte activation in HIV-1 co-infected patients. This might contribute to impaired cellular immune function. Methods: To address this issue we analyzed CD4(+) T absolute counts and the proportion of CD8(+) T cells expressing CD38 in Leishmania/HIV co-infected patients that recovered after anti-leishmanial therapy. Results: We found that, despite clinical remission of leishmaniasis, AVL co-infected patients presented a more severe immunossupression as suggested by CD4(+) T cell counts under 200 cells/mm(3), differing from ATL/HIV-AIDS cases that tends to show higher lymphocytes levels (over 350 cells/mm(3)). Furthermore, five out of nine, AVL/HIV-AIDS presented low CD4(+) T cell counts in spite of low or undetectable viral load. Expression of CD38 on CD8(+) T lymphocytes was significantly higher in AVL or ATL/HIV-AIDS cases compared to HIV/AIDS patients without leishmaniasis or healthy subjects. Conclusions: Leishmania infection can increase the degree of immune system activation in individuals concomitantly infected with HIV. In addition, AVL/HIV-AIDS patients can present low CD4(+) T cell counts and higher proportion of activated T lymphocytes even when HIV viral load is suppressed under HAART. This fact can cause a misinterpretation of these laboratorial markers in co-infected patients.

Ministério da Saúde - Programa Nacional de DST/AIDS

Ministerio da Saude[ED00095/2007]

FIOCRUZ Instituto Oswaldo Cruz

CNPq

(FAPERJ) Fundacao de Amparo a Pesquisa do Estado do Rio de Janeiro

Identificador

BMC INFECTIOUS DISEASES, LONDON, v.10, DEC 10, 2010

1471-2334

http://producao.usp.br/handle/BDPI/15181

10.1186/1471-2334-10-358

http://dx.doi.org/10.1186/1471-2334-10-358

Idioma(s)

eng

Publicador

BIOMED CENTRAL LTD

LONDON

Relação

BMC Infectious Diseases

Direitos

openAccess

Copyright BIOMED CENTRAL LTD

Palavras-Chave #HUMAN-IMMUNODEFICIENCY-VIRUS #AMERICAN CUTANEOUS LEISHMANIASIS #ACTIVE ANTIRETROVIRAL THERAPY #VISCERAL LEISHMANIASIS #IMMUNE-RESPONSES #CELL-ACTIVATION #CD38 EXPRESSION #AIDS #REPLICATION #PATHOGENESIS #Infectious Diseases
Tipo

article

original article

publishedVersion