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  • 1
    Electronic Resource
    Electronic Resource
    Munksgaard : Munksgaard International Publishers
    Journal of clinical periodontology 26 (1999), S. 0 
    ISSN: 1600-051X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract. Patients infected with the human immunodeficiency virus (HIV) are highly susceptible to chronic marginal periodontitis (CMP) and the lesion is generally characterized by abundant plasma cell infiltration. HIV-induced reduction of CD4+ T cells may indirectly affect local production of immunoglobulins (Ig). Gingival biopsies taken from 10 HIV+ and 12 HIV− control patients with CMP were washed, fixed in ethanol and embedded in paraffin. Sections were examined after immunohistochemical staining with monoclonal antibodies against IgA, IgA1–2, IgG, IgG1–4, IgM and IgE. Ig-containing cells were counted in 3 separate connective tissue zones (subjacent to pocket epithelium, central zone and subjacent to oral epithelium). HIV+ patients showed a remarkably increased density of all Ig-containing cells in the connective tissue zone subjacent to the oral epithelium (p〈0.05) and a lower % of IgG2+ cells in the entire gingival section (p〈0.05). In HIV+ patients, the density of IgG-containing cells in the gingiva was strongly correlated with the serum IgG concentration. The altered topical distribution might imply impaired restriction of the inflammatory lesion, additional antigenic challenges by unusual microorganisms in the oral cavity, or be secondary to HIV-induced dysregulation of the B-cell system.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Munksgaard : Munksgaard International Publishers
    Journal of clinical periodontology 26 (1999), S. 0 
    ISSN: 1600-051X
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract. The host immune response in chronic marginal periodontitis (CMP) raised against bacteria colonizing the dentogingival area is modulated by cytokines. This study examines the distribution of the transforming growth factor-β1 containing (TGF-β1 +) cells in formalin-fixed and paraffinembedded gingival specimens from 11 patients with chronic marginal periodontitis and 7 persons with healthy gingiva. Inflamed periodontal tissue contained a 100-fold more TGF-β1 + cells than healthy gingiva. Diverse morphological TGF-β1 + cell types were discerned. Double immuno-enzymatic and -fluorescence staining revealed that TGFβ1 + cells comprised 21–29% macrophages 2–3% T-cells, 3–9% B-cells, 34–35% neutrophilic granulocytes and 7–10% mast cells. The densities of all TGF-β1 + cell types in CMP were strongly increased in the connective tissue adjacent to the pocket epithelium, in the lamina propria and adjacent to the oral epithelium. In lesions with extensive inflammation, expression was also marked in pocket epithelium. TGF-β1 is an immunosuppressive cytokine that stimulates wound healing. Upregulation of the cytokine in inflamed gingiva may counterbalance for destructive gingival inflammatory responses that are simultaneously taking place in patients with CMP.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 38 (1993), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: T-cell receptor γ/δ† (TcRγ/γ†) lymphocytes in human Peyer's patches (PP) adjoining ileal mucosa were studied by monoclonal antibodies with paired immunofluorescence staining in situ and by flowcytomelric phenotyping of isolated cells. The proportion of γδ† T cells in the follicle-associated epithelium outside the M-cell areas (median 4·I%, range 2·2–30·1%,) was similar to that in mucosal villous epithelium (median 4·4%, range 0·5 30·5%). Most intraepithelial °/δ cells (∼90%) expressed CD45RO but only a few expressed CD8 (〈10%) and none l-selectin; a dominating subset (median 46%) employed the Vδl/JδI gene product (range 22–100%). The M-cell areas lacked γ/δ cells but contained clustered CD20+ andCD3+ lymphocytes. Thesubepithelial PP dome area and interfollicular(T-cell) zones, as well as the mucosal lamina propria. contained very few γ/δ cells (median 1·7%, range 0·4–8·9%) which were dominated (88–100%) by the Vγ 2-encoded subset. Those in the dome area and lamina propria were often (∼75%) CD45RO+ (range 44·90%) while very few (∼2%) expressed i.-selectin (range 0·15%). By contrast, CD45RO expression on γ/δ cells in the PPT-cell zones was relatively low (∼46%) and that of l-selectin relatively high (∼43%). In conclusion, TcR γ/δ+ cells are quite rare in human PP and belong mainly to the Vδ2-encoded subset, thus being different from most inlraepithelial γδ cells that probably have another origin. The L-selectin ‘fraction of PPγ/δ cells presumably represent newly recruited ‘naïve’ T lymphocytes while CD45RO+γ/δ cells both in PP and lamina propria arc probably antigen-primed.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: A revived interest in intraepithelial lymphocytes (IEL) has been elicited by several recent reports suggesting that murine and avian intestinal epithelium contains mainly CD3+CD8+ cells expressing the γ/δ T-cell receptor (TcR) for antigen; this contrasts with systemically distributed T cells which preferentially employ the TcRα/β. An anatomical dichotomy in the distribution of these two T-cell lineages has hence been proposed. Here we report that this concept does not hold true in man. In situ studies with monoclonal TcR-framework antibodies showed that most (70–90%) human intestinal IEL (which are mainly CD3+CD8+) expressed TcRα/β. Moreover, almost half of the intraepithelial CD3+ cells were positive for the smallest (180 kDa) CD45 molecule (UCHL1); this probably reflected that they are antigen-primed and thus represent traditional CD3+CD8+α/β+ memory T cells.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 34 (1991), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Fetal (n=20)and postnatal (n = 40) parotid glands were examined by two-colour immunohisto-chemistry combining monoclonal and polyclonal antibody reagents lo study the expression of HLA class I and Il (DR. DP. and DQ). CD45 and CD3, The epithelium lacked class II during fetal life, whereas class I determinants appeared in some acini and most major ducts. Fetal vessels were positive for both class I and class II (mainly DR), suggesting constructive expression. Some class II-positive (DR 〉 DP DQ) histiocytic cells, scaltered CD45+ leucocytes, and very few CD3+ T cells were present in the fetal stroma. The epithelium remained DR-negative the first few weeks after birth, but brisk expression was seen subsequently, DP and DQ remained virtually negative in the epithelium throughout the first year. A slight postnatal increase of class II expression (DR 〉 DP 〉 DQ). along with an apparent decrease in class I. was observed in the endothelium. The number of class Il-positive histiocytic cells. CD45+ leucocytes and CD3+ T cells, as well as the proportion of presumably activated (DR+) T cells, increased a few weeks after birth. The local immune system hence seemed to be stimulated by extrinsic factors, but the overall number of T cells nevertheless remained small. Stimuli other than T cell-derived lymphokines, therefore, probably explained the brisk postnatal epithelial DR induction.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Recent studies in mice and humans have provided evidence for regional specialization of gut intraepithelial lymphocytes (IEL). Here the authors report striking regional variability in the composition of IEL in rat small and large intestine. Two-colour immunofluorescence in situ analysis showed that the distribution of the CD3+ and CD3− IEL subpopulations varied, the proportion of T cells (CD3+) being higher in the ileum than in the jejunum and smallest in the colon. These differences were explained by variable numbers of the T-cell receptor (TCR)α/β+ (both CD8+ and CD4+) but not the TCRγ/δ+ subset. Moreover, the various IEL subpopulations showed distinct intraepithelial distribution patterns with CD4+ and CD8αβ+ T cells situated near the lamina propria, while CD3− IEL were located preferentially towards the adluminal part of the epithelium. Regional phenotypic variation did not depend on intestinal colonization because analogous results were obtained in germ-free rats. Conventionalization nevertheless caused a marked relative increase of small intestinal TCRα/β+ but not TCRγ/δ+ IEL. This increase was more sustained in the jejunum than ileum and eventually reduced the phenotypic IEL differences between the two sites. By contrast, microbial colonization of the colon induced only a transient increase of intraepithelial TCRα/β+ cells with no permanent phenotypic alterations. Both CD3+ and CD3− IEL contained subpopulations that expressed NKR-P1 independent of intestinal colonization. These results demonstrate phenotypic specialization of IEL at different levels of the gut and suggest that the indigenous flora is not essential to this end.
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Jejunal biopsy specimens from 10 patients with treated coeliac disease and seven non-coeliac controls were challenged in vitro with peptic-tryptic gluten digest. Mucosal T cells were examined in situ by three-colour immunofluorescence staining for expression of the activation marker CD25 (the p55 α-chain of intcrlcukin-2 receptor) and the nuclear proliferation marker revealed by monoclonal antibody Ki-67. Intraepithelial T cells expressed CD25 rarely whereas the proportion of activated lamina propria T cells increased (P〈 0.002) from median 2.8% (cultured with 20% fetal calf serum alone for 24–48 h) to 10.0% after 24h with gluten (n= 10; range 1.1–17.4%) and to 10.4% after 48 h (n = 7; range 1.4–17.5%). Such gluten-induced increase of CD25+ T cells was not observed in specimens from non-coeliac control subjects. Crypt-cell hyperplasia and T-cell proliferation (Ki-67+) were observed neither in the coeliac nor in the control mucosae after gluten stimulation. Three-colour staining combining a polyclonal antibody reagent to CD3 and a monoclonal antibody to CD25 with a monoclonal antibody to CD45RO, CD4. CDS, the p75 β-chain of intcrleukin-2 receptor, integrin χEβ7, or HLA-DR showed that most of the CD25+ T cells (〉 90%) were CD4+ CDS, co-expressed CD45RO and the p75 β-chain. and often also the integrin χEβ7 but not HLA–DR. In addition to these activated T cells, a dominating population of CD25+ CD3-CD4+ subepithelial pan-HLA–class I+ macrophages (CD68+) with variable expression of the p75 β-chain was often induced by gluten challenge.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 42 (1995), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Interactions between homing receptors on circulating leucocytes and endothelial addressins regulate tissue-specific cellular extravasation. Although integrin á4β7 appears to be the main receptor for guthoming T lymphocytes, less is known about molecules mediating mucosal B cell homing. Expression of integrin α4β7 on B lymphocytes, B cell blasts, and plasma cells in human gut-associated lymphoid tissue (GALT; the Peyer's patches and appendix) and lamina propria was studied by multi-colour immunofluorescence applied on cryosections. Isolated mononuclear cells from the same tissue compartments were examined by flow cytometry and compared with peripheral blood B cells. Integrin α4β7 was expressed by IgA+ B cell blasts and plasma cells (CD38high) in the lamina propria, B cell blasts in GALT, and sIgD+ B lymphocytes in peripheral blood. In contrast, GALT sIgD+ B lymphocytes were negative or only weakly positive for α4β7. These results suggested that B lymphocytes down-regulate αAβ7 upon extravasation in GALT but up-regulate this integrin after antigen-priming. Thus, α4β7 may be a homing receptor also for B cell blasts extravasating in the gut lamina propria, where this integrin is maintained on plasma cells, perhaps as a local retention factor.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Scandinavian journal of immunology 30 (1989), S. 0 
    ISSN: 1365-3083
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Expression of the γ/δ T-Cell receptor (TcR) for antigen on CD3+ intraepithelial lymphocytes (IEL) was studied in situ by two-colour immunofluorescence on jejunal tissue secretions from 24 patients with coeliac disease and 17 controls. The proportion of intraepithelial TcRγ/δ+ cells was significantly increased (P〈0.002) in untreated (median 20%, range 11–53%) as well in treated (gluten-free diet) coeliac disease (median 23%, range 16–55%) compared with controls (median 2%, range 0–39%). Although TcRγ/β+ IEL dominated both in controls and coeliac disease. T cells expressing the TcRα/δ were preferentially located within the epithelium rather than in the lamina propria. Paired staining for TcRγ/δ and CD8 revealed that most (∼90%) intraepithelial TcRγ/δ+ lymphocytes in coeliac disease were CD8−. A remarkably large fraction (median 67%, range 58–94%) of intraepithelial TcRγ/δ+ cells expressed the Vδ1/Jδ1-encoded epitope revealed by monoclonal antibody δTCS1. Our results suggested that increase of the intraepithelial TcRγ/δ+ CD8− subset of T cells is particularly related to coeliac disease.
    Type of Medium: Electronic Resource
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