2007
DOI: 10.1016/j.cca.2006.05.040
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C-reactive protein in HIV-infected patients—could it be a marker of immunosuppression?

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Cited by 4 publications
(4 citation statements)
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“…C-reactive protein (CRP) is a prophylactic acute-phase plasma protein and a non-specific marker of systemic inflammation that is stimulated by cytokines such as IL-6, IL-1, and TNF to be produced in the liver. The levels of CRP were significantly higher in INRs than that in IRs ( 217 ), and were inversely associated with CD4 + T cell counts ( 192 ). For hypersensitive CRP (hsCRP), there was no difference between INRs and IRs ( 26 ).…”
Section: Soluble Mediators and Cytokinesmentioning
confidence: 99%
“…C-reactive protein (CRP) is a prophylactic acute-phase plasma protein and a non-specific marker of systemic inflammation that is stimulated by cytokines such as IL-6, IL-1, and TNF to be produced in the liver. The levels of CRP were significantly higher in INRs than that in IRs ( 217 ), and were inversely associated with CD4 + T cell counts ( 192 ). For hypersensitive CRP (hsCRP), there was no difference between INRs and IRs ( 26 ).…”
Section: Soluble Mediators and Cytokinesmentioning
confidence: 99%
“…Our study also demonstrates that HIV infection, regardless of pregnancy type does not affect CRP concentration (p = 0.371) with CRP levels being higher in HIV infection than HIV naïve groups. It is controversial that this acute phase protein is elevated in HIV infection compared to HIV naïve patients [42,43]. Previous studies have reported that the high apoptosis, as occurs in HIV infection may promote the production of CRP, a scavenger for chromatin released from apoptotic cells [44,45].…”
Section: -Reactive Proteinmentioning
confidence: 99%
“…9 We also found an increase in the levels of CRP, CD4þ lymphocyte and albumin after 6 months of antiretroviral therapy that interestingly is in line with our previous study. 10 While this study represents the alterations in acutephase proteins among HIV-1 infected persons with and without HAART for over a 6-month follow-up, our study has certain limitations. The study lacks in defining the clinical course of participants especially in regards to describing opportunistic infections, which could likely influence the acute-phase components and the complement system.…”
mentioning
confidence: 96%