Differential cellular recognition pattern to M. tuberculosis targets defined by IFN-γ and IL-17 production in blood from TB plus patients from Honduras as compared to health care workers: TB and immune responses in patients from Honduras

被引:16
作者
Alvarez-Corrales, Nancy [1 ,2 ]
Ahmed, Raija K. [3 ]
Rodriguez, Carol A. [1 ]
Balaji, Kithiganahalli N. [4 ]
Rivera, Rebeca [1 ]
Sompallae, Ramakrishna [5 ]
Vudattu, Nalini K. [6 ]
Hoffner, Sven E. [3 ]
Zumla, Alimuddin [7 ]
Pineda-Garcia, Lelany [1 ]
Maeurer, Markus [2 ,8 ,9 ]
机构
[1] Univ Nacl Autonoma Honduras UNAH, Escuela Microbiol, Tegucigalpa, Honduras
[2] Karolinska Inst, Dept Microbiol Tumor & Cell Biol MTC, Stockholm, Sweden
[3] Swedish Inst Communicable Dis Control SMI, Stockholm, Sweden
[4] Indian Inst Sci, Dept Microbiol & Cell Biol, Bangalore 560012, Karnataka, India
[5] Univ Iowa, Dept Pathol, Iowa City, IA 52242 USA
[6] Yale Univ, Dept Immunobiol, New Haven, CT USA
[7] UCL, Sch Med, Windeyer Inst Med Sci, Dept Infect, London, England
[8] Karolinska Univ Hosp, Ctr Allogene Stem Cell Transplantat CAST, Stockholm, Sweden
[9] Karolinska Inst, Dept Lab Med, Div Therapeut Immunol, Stockholm, Sweden
来源
BMC INFECTIOUS DISEASES | 2013年 / 13卷
关键词
T-cells; M; tuberculosis; TB; Antigen-recognition; Biomarkers; MYCOCEROSIC ACID SYNTHASE; BACILLUS-CALMETTE-GUERIN; COMPLETE GENOME SEQUENCE; MYCOBACTERIUM-BOVIS BCG; 17 CYTOKINE RESPONSES; ESAT-6; FAMILY; MYCOLYL TRANSFERASE; STRUCTURAL-ANALYSIS; VIRULENCE FACTORS; ANTIGEN; 85A;
D O I
10.1186/1471-2334-13-125
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background: A better understanding of the quality of cellular immune responses directed against molecularly defined targets will guide the development of TB diagnostics and identification of molecularly defined, clinically relevant M.tb vaccine candidates. Methods: Recombinant proteins (n = 8) and peptide pools (n = 14) from M. tuberculosis (M.tb) targets were used to compare cellular immune responses defined by IFN-gamma and IL-17 production using a Whole Blood Assay (WBA) in a cohort of 148 individuals, i.e. patients with TB + (n = 38), TB- individuals with other pulmonary diseases (n = 81) and individuals exposed to TB without evidence of clinical TB (health care workers, n = 29). Results: M.tb antigens Rv2958c (glycosyltransferase), Rv2962c (mycolyltransferase), Rv1886c (Ag85B), Rv3804c (Ag85A), and the PPE family member Rv3347c were frequently recognized, defined by IFN-gamma production, in blood from healthy individuals exposed to M.tb (health care workers). A different recognition pattern was found for IL-17 production in blood from M.tb exposed individuals responding to TB10.4 (Rv0288), Ag85B (Rv1886c) and the PPE family members Rv0978c and Rv1917c. Conclusions: The pattern of immune target recognition is different in regard to IFN-gamma and IL-17 production to defined molecular M.tb targets in PBMCs from individuals frequently exposed to M.tb. The data represent the first mapping of cellular immune responses against M.tb targets in TB patients from Honduras.
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页数:11
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