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British journal of biomedical science · 1996

Beta-2-microglobulin, neopterin and monocyte Fc gamma receptors in opportunistic infections of HIV-positive patients.

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Dunne J, Feighery C, Whelan A

Аннотация

The aim of this study was to examine serum and cellular markers of immune activation in HIV-positive (HIV+) patients with and without current opportunistic infections. Fc gamma receptor (Fc gamma R) expression on monocytes, serum neopterin and beta-2-microglobulin were studied. Thirty HIV+ patients (grouped according to Centers for Disease Control (CDC) classification) were studied and compared with 27 normal blood donor controls. HIV+ patients were further separated into three groups: 2 (CDC II), 3 (CDC III/IV without infections) and 4 (CDC III/IV with current infections). Eleven of the patients had current opportunistic infections. Results indicate that beta-microglobulin, neopterin, fc gamma RI, Fc gamma RII and Fc gamma III were significantly increased in HIV+ patients compared to controls. Further analysis of the data using Tukey-Kramer all pairwise comparison revealed that for beta-2-microglobulin the mean values for patients in groups 2, 3 and 4 were significantly different (P < 0.0001). Serum neopterin levels and the percentage of CD14+14+ monocytes expressing Fc gamma RIII showed significant differences in the mean values of group 2 and group 4; similarly, for CD4+ lymphocyte counts group 2 and group 4 were significantly different. These results indicated that beta-2-microglobulin, neopterin and CD14+ monocyte Fc gamma RIII are increased particularly in HIV+ patients with current opportunistic infections while CD4+ lymphocyte counts are reduced. The results suggest that these markers, particularly beta-2-microglobulin, could be useful indicators of the inflammatory process associated with opportunistic infection at later stages of disease where other laboratory markers may be atypical.

Предметные рубрики MeSH

ИП Урсолов Владлен Сергеевич

ИНН 500118482352 · ОГРНИП 314500117700049

Реквизиты и контакты