T-cell-receptor gene usage of Actinobacillus actinomycetemcomitans-reactive periodontal CD4+ T cells from localized juvenile periodontitis patients and human peripheral blood leukocyte-reconstituted NOD/SCID mice

We investigated the variable Vα and Vβ gene usage of Actinobacillus actinomycetemcomitans‐reactive periodontal CD4+ T cell receptors (TCR) from: (i) four A. actinomycetemcomitans‐infected localized juvenile periodontitis (LJP) patients, (ii) four groups of A. actinomycetemcomitans‐inoculated NOD/SCI...

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Published inJournal of periodontal research Vol. 37; no. 5; pp. 399 - 404
Main Authors Gao, Xuijuan, Teng, Yen-Tung A.
Format Journal Article
LanguageEnglish
Published Oxford, UK Munksgaard International Publishers 01.10.2002
Blackwell
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ISSN0022-3484
1600-0765
DOI10.1034/j.1600-0765.2002.01006.x

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Abstract We investigated the variable Vα and Vβ gene usage of Actinobacillus actinomycetemcomitans‐reactive periodontal CD4+ T cell receptors (TCR) from: (i) four A. actinomycetemcomitans‐infected localized juvenile periodontitis (LJP) patients, (ii) four groups of A. actinomycetemcomitans‐inoculated NOD/SCID mice engrafted with individual LJP‐derived HuPBL and (iii) HuPBL samples of four LJP patients and two healthy control subjects, by quantitative PCR analyses. The results show that: (i) the majority of the TCR genes (82.5% of Vα and 91.1% of Vβ) used by periodontal CD4+ T cells in A. actinomycetemcomitans‐inoculated HuPBL‐engrafted NOD/SCID mice overlap with those used by local periodontal T cells in LJP patients, (ii) although A. actinomycetemcomitans‐reactive periodontal CD4+ TCR repertoire is relatively widespread, there are a few dominant genes shared by the LJP patients, suggesting a limited number of antigens or epitopes commonly recognized and (iii) A. actinomycetemcomitans likely lacks superantigenic characteristics. These results suggest A. actinomycetemcomitans‐associated human CD4+ T cell repertoire established in HuPBL‐NOD/SCID mice provides a useful approach to study specific aspects of immune–parasite interactions in the periodontium.
AbstractList We investigated the variable Vα and Vβ gene usage of Actinobacillus actinomycetemcomitans ‐reactive periodontal CD4 + T cell receptors (TCR) from: (i) four A. actinomycetemcomitan s‐infected localized juvenile periodontitis (LJP) patients, (ii) four groups of A. actinomycetemcomitans ‐inoculated NOD/SCID mice engrafted with individual LJP‐derived HuPBL and (iii) HuPBL samples of four LJP patients and two healthy control subjects, by quantitative PCR analyses. The results show that: (i) the majority of the TCR genes (82.5% of Vα and 91.1% of Vβ) used by periodontal CD4 + T cells in A. actinomycetemcomitans ‐inoculated HuPBL‐engrafted NOD/SCID mice overlap with those used by local periodontal T cells in LJP patients, (ii) although A. actinomycetemcomitans ‐reactive periodontal CD4 + TCR repertoire is relatively widespread, there are a few dominant genes shared by the LJP patients, suggesting a limited number of antigens or epitopes commonly recognized and (iii) A. actinomycetemcomitans likely lacks superantigenic characteristics. These results suggest A. actinomycetemcomitans ‐associated human CD4 + T cell repertoire established in HuPBL‐NOD/SCID mice provides a useful approach to study specific aspects of immune–parasite interactions in the periodontium.
We investigated the variable Valpha and Vbeta gene usage of Actinobacillus actinomycetemcomitans-reactive periodontal CD4+ T cell receptors (TCR) from: (i) four A. actinomycetemcomitans-infected localized juvenile periodontitis (LJP) patients, (ii) four groups of A. actinomycetemcomitans-inoculated NOD/SCID mice engrafted with individual LJP-derived HuPBL and (iii) HuPBL samples of four LJP patients and two healthy control subjects, by quantitative PCR analyses. The results show that: (i) the majority of the TCR genes (82.5% of Valpha and 91.1% of Vbeta) used by periodontal CD4+ T cells in A. actinomycetemcomitans-inoculated HuPBL-engrafted NOD/SCID mice overlap with those used by local periodontal T cells in LJP patients, (ii) although A. actinomycetemcomitans-reactive periodontal CD4+ TCR repertoire is relatively widespread, there are a few dominant genes shared by the LJP patients, suggesting a limited number of antigens or epitopes commonly recognized and (iii) A. actinomycetemcomitans likely lacks superantigenic characteristics. These results suggest A. actinomycetemcomitans-associated human CD4+ T cell repertoire established in HuPBL-NOD/SCID mice provides a useful approach to study specific aspects of immune-parasite interactions in the periodontium.We investigated the variable Valpha and Vbeta gene usage of Actinobacillus actinomycetemcomitans-reactive periodontal CD4+ T cell receptors (TCR) from: (i) four A. actinomycetemcomitans-infected localized juvenile periodontitis (LJP) patients, (ii) four groups of A. actinomycetemcomitans-inoculated NOD/SCID mice engrafted with individual LJP-derived HuPBL and (iii) HuPBL samples of four LJP patients and two healthy control subjects, by quantitative PCR analyses. The results show that: (i) the majority of the TCR genes (82.5% of Valpha and 91.1% of Vbeta) used by periodontal CD4+ T cells in A. actinomycetemcomitans-inoculated HuPBL-engrafted NOD/SCID mice overlap with those used by local periodontal T cells in LJP patients, (ii) although A. actinomycetemcomitans-reactive periodontal CD4+ TCR repertoire is relatively widespread, there are a few dominant genes shared by the LJP patients, suggesting a limited number of antigens or epitopes commonly recognized and (iii) A. actinomycetemcomitans likely lacks superantigenic characteristics. These results suggest A. actinomycetemcomitans-associated human CD4+ T cell repertoire established in HuPBL-NOD/SCID mice provides a useful approach to study specific aspects of immune-parasite interactions in the periodontium.
We investigated the variable Vα and Vβ gene usage of Actinobacillus actinomycetemcomitans‐reactive periodontal CD4+ T cell receptors (TCR) from: (i) four A. actinomycetemcomitans‐infected localized juvenile periodontitis (LJP) patients, (ii) four groups of A. actinomycetemcomitans‐inoculated NOD/SCID mice engrafted with individual LJP‐derived HuPBL and (iii) HuPBL samples of four LJP patients and two healthy control subjects, by quantitative PCR analyses. The results show that: (i) the majority of the TCR genes (82.5% of Vα and 91.1% of Vβ) used by periodontal CD4+ T cells in A. actinomycetemcomitans‐inoculated HuPBL‐engrafted NOD/SCID mice overlap with those used by local periodontal T cells in LJP patients, (ii) although A. actinomycetemcomitans‐reactive periodontal CD4+ TCR repertoire is relatively widespread, there are a few dominant genes shared by the LJP patients, suggesting a limited number of antigens or epitopes commonly recognized and (iii) A. actinomycetemcomitans likely lacks superantigenic characteristics. These results suggest A. actinomycetemcomitans‐associated human CD4+ T cell repertoire established in HuPBL‐NOD/SCID mice provides a useful approach to study specific aspects of immune–parasite interactions in the periodontium.
We investigated the variable Valpha and Vbeta gene usage of Actinobacillus actinomycetemcomitans-reactive periodontal CD4+ T cell receptors (TCR) from: (i) four A. actinomycetemcomitans-infected localized juvenile periodontitis (LJP) patients, (ii) four groups of A. actinomycetemcomitans-inoculated NOD/SCID mice engrafted with individual LJP-derived HuPBL and (iii) HuPBL samples of four LJP patients and two healthy control subjects, by quantitative PCR analyses. The results show that: (i) the majority of the TCR genes (82.5% of Valpha and 91.1% of Vbeta) used by periodontal CD4+ T cells in A. actinomycetemcomitans-inoculated HuPBL-engrafted NOD/SCID mice overlap with those used by local periodontal T cells in LJP patients, (ii) although A. actinomycetemcomitans-reactive periodontal CD4+ TCR repertoire is relatively widespread, there are a few dominant genes shared by the LJP patients, suggesting a limited number of antigens or epitopes commonly recognized and (iii) A. actinomycetemcomitans likely lacks superantigenic characteristics. These results suggest A. actinomycetemcomitans-associated human CD4+ T cell repertoire established in HuPBL-NOD/SCID mice provides a useful approach to study specific aspects of immune-parasite interactions in the periodontium.
Author Teng, Yen-Tung A.
Gao, Xuijuan
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Keywords Immune response
Pathophysiology
Stomatology
Leukocyte
Rodentia
Receiver
Experimental study
Pasteurellaceae
Polymerase chain reaction
Periodontal disease
Vertebrata
Mammalia
Mouse
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Snippet We investigated the variable Vα and Vβ gene usage of Actinobacillus actinomycetemcomitans‐reactive periodontal CD4+ T cell receptors (TCR) from: (i) four A....
We investigated the variable Vα and Vβ gene usage of Actinobacillus actinomycetemcomitans ‐reactive periodontal CD4 + T cell receptors (TCR) from: (i) four A....
We investigated the variable Valpha and Vbeta gene usage of Actinobacillus actinomycetemcomitans-reactive periodontal CD4+ T cell receptors (TCR) from: (i)...
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SubjectTerms Actinobacillus actinomycetemcomitans
Aggregatibacter actinomycetemcomitans - immunology
Aggressive Periodontitis - genetics
Aggressive Periodontitis - immunology
Aggressive Periodontitis - microbiology
Animals
Antigens, Bacterial - genetics
Antigens, Bacterial - immunology
Biological and medical sciences
CD4-Positive T-Lymphocytes - immunology
CD4-Positive T-Lymphocytes - metabolism
Epitopes - genetics
Epitopes - immunology
Facial bones, jaws, teeth, parodontium: diseases, semeiology
Female
Genes, T-Cell Receptor alpha - genetics
Genes, T-Cell Receptor beta - genetics
Humans
HuPBL-NOD/SCID mice
immune repertoire
Leukocytes - immunology
Leukocytes - metabolism
localized juvenile periodontitis
Male
Medical sciences
Mice
Mice, Inbred NOD
Mice, SCID
Non tumoral diseases
Otorhinolaryngology. Stomatology
Polymerase Chain Reaction
Receptors, Antigen, T-Cell - genetics
Superantigens - genetics
T-cell-receptor genes
Title T-cell-receptor gene usage of Actinobacillus actinomycetemcomitans-reactive periodontal CD4+ T cells from localized juvenile periodontitis patients and human peripheral blood leukocyte-reconstituted NOD/SCID mice
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https://www.ncbi.nlm.nih.gov/pubmed/12366864
https://www.proquest.com/docview/72156018
Volume 37
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