دورية أكاديمية

Role of TEFFECTOR/MEMORY Cells, TBX21 Gene Expression and T-Cell Homing Receptor on Type 1 Reaction in Borderline Lepromatous Leprosy Patients.

التفاصيل البيبلوغرافية
العنوان: Role of TEFFECTOR/MEMORY Cells, TBX21 Gene Expression and T-Cell Homing Receptor on Type 1 Reaction in Borderline Lepromatous Leprosy Patients.
المؤلفون: Dos Santos LN; Leprosy Laboratory, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil., da Silva PH; Leprosy Laboratory, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil., Alvim IM; Laboratory of Cellular Microbiology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil., Nery JA; Leprosy Laboratory, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil., Lara FA; Laboratory of Cellular Microbiology, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil., Sarno EN; Leprosy Laboratory, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil., Esquenazi D; Leprosy Laboratory, Oswaldo Cruz Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.; Department of Pathology and Laboratories, School of Medical Sciences, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
المصدر: PloS one [PLoS One] 2016 Oct 20; Vol. 11 (10), pp. e0164543. Date of Electronic Publication: 2016 Oct 20 (Print Publication: 2016).
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet ISSN: 1932-6203 (Electronic) Linking ISSN: 19326203 NLM ISO Abbreviation: PLoS One Subsets: MEDLINE
أسماء مطبوعة: Original Publication: San Francisco, CA : Public Library of Science
مواضيع طبية MeSH: CD4-Positive T-Lymphocytes/*metabolism , CD8-Positive T-Lymphocytes/*metabolism , Leprosy/*immunology , Receptors, Lymphocyte Homing/*metabolism , T-Box Domain Proteins/*metabolism, Adolescent ; Adult ; Aged ; Antigens, Differentiation, T-Lymphocyte/genetics ; Antigens, Differentiation, T-Lymphocyte/metabolism ; Female ; Humans ; Leprosy/genetics ; Leprosy/metabolism ; Male ; Membrane Glycoproteins/genetics ; Membrane Glycoproteins/metabolism ; Middle Aged ; Receptors, Lymphocyte Homing/genetics ; T-Box Domain Proteins/genetics ; Up-Regulation ; Young Adult
مستخلص: In spite of hyporesponsivity to Mycobacterium leprae, borderline lepromatous (BL) patients show clinical and immunological instability, and undergo frequent acute inflammatory episodes such as type 1 reaction (T1R), which may cause nerve damages. This work focused on the participation of T cell subsets from blood and skin at T1R onset. We observed a significantly increased ex vivo frequency of both effector and memory CD4+ and CD8+ T cells in T1R group. Besides, ex vivo frequency of T cell homing receptor, the Cutaneous Leukocyte-associated Antigen (CLA) was significantly increased in T cells from T1R patients. M. leprae induced a higher frequency of CD4+ TEM and CD8+ TEF cells, as well as of CD8+/TEMRA (terminally differentiated effector T cells) subset, which expressed high CD69+. The presence of IFN-γ‒producing-CD4+ TEF and naïve and effector CD8+ T lymphocytes was significant in T1R. TBX21 expression was significantly higher in T1R, while BL showed increased GATA3 and FOXP3 expression. In T1R, TBX21 expression was strongly correlated with CD8+/IFN-γ‒ T cells frequency. The number of double positive CD8+/CLA+ and CD45RA+/CLA+ cells was significantly higher in skin lesions from T1R, in comparison with non-reactional BL group. The observed increase of ex vivo T cells at T1R onset suggests intravascular activation at the beginning of reactional episodes. The antigen-specific response in T1R group confirmed the higher number of CD8+/CLA+ and CD45RA+/CLA+ cells in T1R lesions suggests possible migration of these cells activated by M. leprae components inside the vascular compartment to skin and participation in T1R physiopathology.
Competing Interests: The authors have declared that no competing interests exist.
References: Eur J Immunol. 2014 Feb;44(2):431-9. (PMID: 24214631)
Br J Dermatol. 2015 Jan;172(1):268-71. (PMID: 25256168)
PLoS Negl Trop Dis. 2012;6(4):e1616. (PMID: 22545169)
Appl Microbiol Biotechnol. 2016 Apr;100(7):3267-75. (PMID: 26820649)
PLoS Pathog. 2013;9(7):e1003504. (PMID: 23874205)
Clin Dermatol. 2015 Jan-Feb;33(1):26-37. (PMID: 25432808)
Lepr Rev. 2008 Dec;79(4):372-86. (PMID: 19274984)
PLoS Negl Trop Dis. 2016 Apr 01;10(4):e0004592. (PMID: 27035913)
PLoS Negl Trop Dis. 2011 Dec;5(12):e1327. (PMID: 22180790)
Annu Rev Immunol. 2013;31:137-61. (PMID: 23215646)
J Immunol. 1993 Jun 15;150(12):5501-10. (PMID: 8515073)
J Immunol. 1997 Nov 1;159(9):4474-83. (PMID: 9379047)
Int J Lepr Other Mycobact Dis. 1994 Dec;62(4):559-67. (PMID: 7868954)
Am J Trop Med Hyg. 2012 May;86(5):878-83. (PMID: 22556091)
Braz J Med Biol Res. 1998 Jan;31(1):69-76. (PMID: 9686181)
Clin Exp Immunol. 2003 Dec;134(3):447-53. (PMID: 14632750)
Scand J Immunol. 2000 Apr;51(4):419-28. (PMID: 10736116)
J Immunol. 2004 Sep 15;173(6):4120-9. (PMID: 15356162)
Immunology. 1998 Dec;95(4):529-36. (PMID: 9893041)
Clin Immunol. 2014 Apr;151(2):84-99. (PMID: 24584041)
Nat Immunol. 2010 Aug;11(8):674-80. (PMID: 20644573)
J Immunol. 2015 Apr 1;194(7):2961-75. (PMID: 25795787)
Wkly Epidemiol Rec. 2015 Sep 2;91(35):405-20. (PMID: 27592500)
Clin Exp Immunol. 1984 Mar;55(3):623-8. (PMID: 6423326)
Clin Exp Immunol. 1991 Apr;84(1):103-8. (PMID: 2015700)
Clin Exp Dermatol. 2008 May;33(3):294-7. (PMID: 18261142)
Infect Immun. 1992 Apr;60(4):1441-6. (PMID: 1548069)
J Immunol. 2011 Nov 15;187(10):4967-78. (PMID: 21987662)
Rev Inst Med Trop Sao Paulo. 1998 Nov-Dec;40(6):363-70. (PMID: 10436656)
Immunology. 2013 Sep;140(1):47-60. (PMID: 23566249)
J Immunol. 2007 Aug 15;179(4):2389-96. (PMID: 17675500)
Int J Lepr Other Mycobact Dis. 1966 Jul-Sep;34(3):255-73. (PMID: 5950347)
Nature. 1999 Oct 14;401(6754):708-12. (PMID: 10537110)
J Immunol Methods. 2003 Jul;278(1-2):157-69. (PMID: 12957404)
Immunology. 2007 Apr;120(4):518-25. (PMID: 17343614)
J Clin Immunol. 2013 Jan;33(1):220-34. (PMID: 22990666)
Clin Exp Immunol. 2009 Sep;157(3):377-84. (PMID: 19664146)
Expert Rev Clin Immunol. 2015 Mar;11(3):391-407. (PMID: 25666357)
BMC Infect Dis. 2009 May 27;9:75. (PMID: 19473542)
J Clin Immunol. 2014 Feb;34(2):245-55. (PMID: 24370984)
PLoS One. 2015 Sep 04;10(9):e0136282. (PMID: 26340474)
Eur J Immunol. 2012 Nov;42(11):2925-36. (PMID: 22851198)
An Bras Dermatol. 2013 Sep-Oct;88(5):787-92. (PMID: 24173185)
Scand J Immunol. 1999 Nov;50(5):541-9. (PMID: 10564558)
J Invest Dermatol. 1999 Nov;113(5):752-9. (PMID: 10571730)
Clin Vaccine Immunol. 2011 Jun;18(6):947-53. (PMID: 21508169)
J Infect. 2010 Feb;60(2):133-9. (PMID: 19878691)
Mucosal Immunol. 2011 May;4(3):261-70. (PMID: 21451501)
المشرفين على المادة: 0 (Antigens, Differentiation, T-Lymphocyte)
0 (CTAGE1 protein, human)
0 (Membrane Glycoproteins)
0 (Receptors, Lymphocyte Homing)
0 (T-Box Domain Protein 2)
0 (T-Box Domain Proteins)
0 (T-box transcription factor TBX21)
تواريخ الأحداث: Date Created: 20161021 Date Completed: 20170605 Latest Revision: 20181113
رمز التحديث: 20231215
مُعرف محوري في PubMed: PMC5072666
DOI: 10.1371/journal.pone.0164543
PMID: 27764137
قاعدة البيانات: MEDLINE
الوصف
تدمد:1932-6203
DOI:10.1371/journal.pone.0164543