z-logo
open-access-imgOpen Access
Normal CD16 Expression and Phagocytosis ofMycobacterium aviumComplex by Monocytes from a Current Cohort of HIV‐1–Infected Patients
Author(s) -
Anthony Jaworowski,
Philip Ellery,
Clare Maslin,
Eman Naim,
Amy Candy Heinlein,
Claire Ryan,
Geza Paukovics,
Jane S. Hocking,
Secondo Sonza,
Suzanne M. Crowe
Publication year - 2006
Publication title -
the journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/500367
Subject(s) - phagocytosis , cd16 , human immunodeficiency virus (hiv) , immunology , cohort , mycobacterium avium complex , nontuberculous mycobacteria , microbiology and biotechnology , monocyte , macrophage , virology , medicine , biology , mycobacterium , immune system , tuberculosis , pathology , in vitro , genetics , cd3 , cd8
Monocyte phenotype and function were measured in whole blood sampled from a current cohort of human immunodeficiency virus (HIV)-infected individuals attending a large, metropolitan, university-affiliated hospital. There was no significant difference in the prevalence of CD16+ monocytes or the capacity of monocytes to ingest heat-killed Mycobacterium avium complex between these individuals and HIV-uninfected control subjects, regardless of viral load, current CD4+ T cell count, nadir CD4+ T cell count, or time since diagnosis of HIV infection. CD16+ monocyte prevalence was, however, elevated in patients not currently receiving antiretroviral therapy. We conclude that HIV type 1 infection in the setting of highly active antiretroviral therapy is associated with normal monocyte function and phenotype.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom