1997
DOI: 10.1046/j.1365-3083.1997.d01-413.x
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Characterization of Chlamydia pneumoniae Antigens Using Human T Cell Clones

Abstract: Halme S, Saikku P, Surcel H-M. Characterization of Chlamydia pneumoniae Antigens Using Human T Cell Clones. Scand J Immunol 1997;45:378-384 Chlamydia pneumoniae infection is followed by the development of antigen-specific cell-mediated immunity (CMI), which is detectable as a positive lymphocyte proliferation (LP) response to C. pneumoniae elementary body (EB) antigen, but the proteins inducing the T cell activation are not known. In the present work the authors used human T lymphocyte clones (TLC) raised a… Show more

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Cited by 25 publications
(18 citation statements)
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References 28 publications
(55 reference statements)
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“…Since the interaction in the risk for EH of one allele of the HLA system (a key element of the immune response) and an infectious agent (C. pneumoniae) has been described in our study, the probability that immune and inflammatory mechanisms are important factors in the pathogenesis of EH (as has been well documented in atherosclerosis at the cellular 21 and biochemical level 22 ) is clearly higher than that previously suspected. On the basis of several experimental findings, [23][24][25][26][27][28] it has been hypothesized that chronic C. pneumoniae infection of the vessels may induce a chronic immune response orchestrated by cytokines and mediated by reactive oxygen intermediates. This may result in increased vascular resistance and lead to increased blood pressure.…”
Section: Discussionmentioning
confidence: 99%
“…Since the interaction in the risk for EH of one allele of the HLA system (a key element of the immune response) and an infectious agent (C. pneumoniae) has been described in our study, the probability that immune and inflammatory mechanisms are important factors in the pathogenesis of EH (as has been well documented in atherosclerosis at the cellular 21 and biochemical level 22 ) is clearly higher than that previously suspected. On the basis of several experimental findings, [23][24][25][26][27][28] it has been hypothesized that chronic C. pneumoniae infection of the vessels may induce a chronic immune response orchestrated by cytokines and mediated by reactive oxygen intermediates. This may result in increased vascular resistance and lead to increased blood pressure.…”
Section: Discussionmentioning
confidence: 99%
“…The pathophysiology of this immunodeficiency is probably multifactorial. Data from experimental studies suggest that the T-cell repertoire in CTCL patients is significantly contracted [27] Immunological abnormalities in CTCL are typically associated with depressed ability of peripheral blood cells to produce the Th 1 cytokines, interferon gamma and IL-2 as a result of Th 2 skewing. [28][29][30][31][32][33][34][35][36][37] During CTCL progression, reduced T-cell-mediated cellular immune responses and diminished natural killer cell activity also develop [38,39] Wysocka et al have demonstrated a direct relationship between the extend of the pool of circulating malignant T-cells and an impaired immune response [40].…”
Section: Discussionmentioning
confidence: 99%
“…Although chlamydial elementary body (EB) contains dozens of proteins that are able to elicit lymphocyte proliferation [47], as many as 30% of the C. trachomatis-specific T-cell clones recognized chlamydial HSP60, suggesting that it is a relatively important antigen for the induction of cellular responses in the salpingeal tissue of TFI patients [Kinnunen and coauthors, unpublished observations].…”
Section: Chlamydia Hsp60 Specific T-cell Response In Humansmentioning
confidence: 99%