» Articles » PMID: 1356262

CD45RA and CD45RO Positive CD4 Cells in Human Peripheral Blood and Periodontal Disease Tissue Before and After Stimulation with Periodontopathic Bacteria

Overview
Date 1992 Apr 1
PMID 1356262
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Flow cytometric analysis was used to examine naive and primed or memory CD4 cells extracted from periodontal lesions compared with cells from peripheral blood of healthy subjects before and after stimulation with the periodontopathic bacteria, Porphyromonas gingivalis and Fusobacterium nucleatum. In peripheral blood, approximately 60% and 40% of CD4 cells were CD45RO+ and CD45RA+ respectively at day 0. Phytohaemagglutinin (PHA) induced CD45RO expression on almost 100% of CD4 cells. However, P. gingivalis and F. nucleatum stimulation did not cause any significant change in percentage of CD45RO+ CD4 cells except for a loss of antigen at day 6 together with re-expression at day 7, which also occurred on cells cultured in medium only. CD45RA expression on PHA and bacterial-stimulated peripheral blood CD4 cells remained fairly stable for the 10-d culture period. Greater than 90% CD4 cells extracted from healthy or marginal gingivitis (H/MG) and adult periodontitis (AP) lesions were CD45RO+ and this was maintained on AP cells throughout the 6-d culture period, except for a small decrease in the percentage of positive cells induced by P. gingivalis at day 3. Approximately 9% CD4 cells from H/MG tissue were CD45RA+, but about 22% AP cells expressed this antigen, and this increased again in P. gingivalis- and F. nucleatum-stimulated cultures after 3 d. Therefore, in peripheral blood P. gingivalis and F. nucleatum do not act as nonspecific T-cell mitogens and, in AP cells, these bacteria induce changes in phenotype, supporting previous data that although they may be polyclonal B-cell activators, they activate antigen specific T-cells.

Citing Articles

Maintaining homeostatic control of periodontal bone tissue.

Hathaway-Schrader J, Novince C Periodontol 2000. 2021; 86(1):157-187.

PMID: 33690918 PMC: 8294452. DOI: 10.1111/prd.12368.


Lymphocyte subpopulation in healthy and diseased gingival tissue.

Amunulla A, Venkatesan R, Ramakrishnan H, Arun K, Sudarshan S, Talwar A J Indian Soc Periodontol. 2010; 12(2):45-50.

PMID: 20142944 PMC: 2813557. DOI: 10.4103/0972-124X.44091.


Macrophage inflammatory protein 3alpha-CC chemokine receptor 6 interactions play an important role in CD4+ T-cell accumulation in periodontal diseased tissue.

Hosokawa Y, Nakanishi T, Yamaguchi D, Takahashi K, Yumoto H, Ozaki K Clin Exp Immunol. 2002; 128(3):548-54.

PMID: 12067311 PMC: 1906256. DOI: 10.1046/j.1365-2249.2002.01865.x.


Selective expansion of T cells in gingival lesions of patients with chronic inflammatory periodontal disease.

Yamazaki K, Nakajima T, Ohsawa Y, Tabeta K, Yoshie H, Sakurai K Clin Exp Immunol. 2000; 120(1):154-61.

PMID: 10759777 PMC: 1905632. DOI: 10.1046/j.1365-2249.2000.01179.x.


Differential expression of costimulatory molecules in chronic inflammatory periodontal disease tissue.

Orima K, Yamazaki K, Aoyagi T, Hara K Clin Exp Immunol. 1999; 115(1):153-60.

PMID: 9933436 PMC: 1905181. DOI: 10.1046/j.1365-2249.1999.00763.x.