Published February 5, 2010 | Version v1
Journal article Open

Significant CD4, CD8, and CD19 Lymphopenia in Peripheral Blood of Sarcoidosis Patients Correlates with Severe Disease Manifestations

  • 1. University of Chicago
  • 2. Methodist Hospital
  • 3. University of Cincinnati Medical Center
  • 4. Johns Hopkins University

Description

Background: Sarcoidosis is a poorly understood chronic inflammatory condition. Infiltration of affected organs by lymphocytes is characteristic of sarcoidosis, however previous reports suggest that circulating lymphocyte counts are low in some patients with the disease. The goal of this study was to evaluate lymphocyte subsets in peripheral blood in a cohort of sarcoidosis patients to determine the prevalence, severity, and clinical features associated with lymphopenia in major lymphocyte subsets.

Methodology/Principal Findings: Lymphocyte subsets in 28 sarcoid patients were analyzed using flow cytometry to determine the percentage of CD4, CD8, and CD19 positive cells. Greater than 50% of patients had abnormally low CD4, CD8, or CD19 counts (p<4×10−10). Lymphopenia was profound in some cases, and five of the patients had absolute CD4 counts below 200. CD4, CD8, and CD19 lymphocyte subset counts were significantly correlated (Spearman's rho 0.57, p = 0.0017), and 10 patients had low counts in all three subsets. Patients with severe organ system involvement including neurologic, cardiac, ocular, and advanced pulmonary disease had lower lymphocyte subset counts as a group than those patients with less severe manifestations (CD4 p = 0.0043, CD8 p = 0.026, CD19 p = 0.033). No significant relationships were observed between various medical therapies and lymphocyte counts, and lymphopenia was present in patients who were not receiving any medical therapy.

Conclusions/Significance Significant lymphopenia involving CD4, CD8, and CD19 positive cells was common in sarcoidosis patients and correlated with disease severity. Our findings suggest that lymphopenia relates more to disease pathology than medical treatment.

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Additional details

Identifiers

DOI
10.1371/journal.pone.0009088
Other
oai:uchicago.tind.io:8210

Funding

National Institutes of Health
K08 AI083790
NIAID
Clinical Research Loan Repayment
Arthritis National Research Foundation
Eng Tan Scholar Award
Lupus Research Institute
University of Chicago/Northshore University Health System
Translational Research Pilot Grant
Abbott
Genentech
BMS
Unknown funder
Young investigator award
Foundation for Sarcoidosis Research

UChicago Information

Division(s)
Biological Sciences Division
Department(s)
Medicine