Affiliation:
1. Departments of Dermatology1 and
2. Pathology and Laboratory Medicine,2 Medical College of Pennsylvania and Hahnemann University, Philadelphia, Pennsylvania 19102-1192
Abstract
ABSTRACT
We previously identified a protein that was stimulatory for malignant Sézary T cells, termed Sézary T-cell activating factor (SAF). However, the identity of this protein has not been fully elucidated, nor has it’s role been determined in the pathogenesis of cutaneous T-cell lymphoma (CTCL). The basis for epidermotropism and proliferation of malignant cells in the skin of patients with CTCL is unknown. Using a monoclonal antibody inhibitory for SAF activity, we demonstrated that SAF is present in the skin of 16 of 27 samples from patients with mycosis fungoides, the predominant form of CTCL. In this report, the SAF determinant is demonstrated to be associated with
Chlamydia pneumoniae
bacteria by immunohistochemistry, immunoelectron microscopy, and culture analysis. Reactivity of antibodies against an outer membrane protein of
C. pneumoniae
or against the lipopolysaccharide of
Chlamydiae
spp. demonstrated that these determinants are coexpressed in 90% of the SAF-positive samples. We confirmed the presence of
C. pneumoniae
DNA and RNA in the skin by PCR and reverse transcription-PCR and by sequence analysis of the PCR products. The expression of the
C. pneumoniae
antigens and SAF appears to be associated with active disease in that
C. pneumoniae
antigens were absent or greatly diminished in the skin of three patients examined after Psoralen and long-wave UVA radiation treatment. Our results suggest that SAF is a
Chlamydia
-associated protein and that further investigation is warranted to determine whether SAF and
C. pneumoniae
play a role in the pathogenesis of CTCL.
Publisher
American Society for Microbiology
Subject
Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy
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