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Clinical Immunophenotype at Disease Onset in Previously Healthy Patients With Cryptococcal Meningitis. | LitMetric

Clinical Immunophenotype at Disease Onset in Previously Healthy Patients With Cryptococcal Meningitis.

Medicine (Baltimore)

From the Department of Infectious Disease (LX, QH, C-YZ, S-KY, A-HZ, YL), Medical Inspection Department (D-HC), Department of Hepatology, Shanghai Public Health Clinical Center (LC); Dermatological Department, Huashan Hospital, Fudan University, Shanghai (J-RL, C-FZ); and Department of Infectious Diseases (X-HL), The Third Affiliated Hospital of Sun-Yat-Sen University, Guangzhou, China.

Published: February 2016

AI Article Synopsis

  • Cryptococcal meningitis (CM) is a serious global disease affecting both HIV-infected and previously healthy patients, yet the immune responses in previously healthy patients (PHPs) are not well understood.
  • A study analyzing 41 CM patients found that PHPs had higher counts of certain immune cells compared to non-PHPs, but similar levels of inflammatory markers, aside from lower immunoglobulin A (IgA) in non-PHPs.
  • Despite PHPs having a higher five-year mortality rate than non-PHPs (22% vs. 12.5%), this difference was not statistically significant; however, higher immunoglobulin G (IgG) levels in serum during the disease onset may indicate increased mortality

Article Abstract

Cryptococcal meningitis (CM) is a global disease with significant morbidity and mortality. Although low peripheral blood cluster of differentiation 4 (CD4) cell counts are found to be related to a high burden of cryptococcus in HIV-infected patients, little is known about possible immune defects in previously healthy patients (PHPs). We performed a retrospective study of 41 CM patients treated from January 2005 to December 2014 who did not have HIV-infection. There were 33 PHPs and 8 not previously healthy patients (non-PHPs). We analyzed clinical test data pertaining to peripheral blood T cells, antibodies, inflammation markers, and cerebral spinal fluid (CSF) completed during the disease onset phase and 5 years following diagnosis. PHPs had significantly higher counts of cluster of differentiation 3 (CD3), cluster of differentiation 4 (CD4), and cluster of differentiation 45 (CD45) cells, and lower percentages of CD8 cells than non-PHPs (P < 0.05). Measurements of inflammatory markers and immunoglobulin in blood were comparable except for lower immunoglobulin A (IgA) levels in non-PHPs (P = 0.0410). Examination of CSF revealed lower white blood cell (WBC) counts in non-PHPs. Five-year mortality in PHPs was higher than in non-PHPs (22.0% vs 12.5%) but this was not statistically significant (P > 0.05). Multivariate analysis revealed that higher immunoglobulin G (IgG) levels in serum during disease onset may be an independent predictor of mortality (P = 0.015). In conclusion, PHPs demonstrate an immunophenotype that is distinct from that of non-PHPs, leading to an improved understanding of the immunology of cryptococcal meningitis.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4753916PMC
http://dx.doi.org/10.1097/MD.0000000000002744DOI Listing

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