IgA and IgG against Mycobacterium tuberculosis Rv2031 discriminate between pulmonary tuberculosis patients, Mycobacterium tuberculosis-infected and non-infected individuals.
IgA and IgG against Mycobacterium tuberculosis Rv2031 discriminate between pulmonary tuberculosis patients, Mycobacterium tuberculosis-infected and non-infected individuals.
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针对结核分枝杆菌RV2031的IgA和IgG区分肺结核患者,结核分枝杆菌感染和未感染的个体。
DOI:
10.1371/journal.pone.0190989
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发表时间:
2018
期刊:
影响因子:
3.7
通讯作者:
Ottenhoff THM
中科院分区:
文献类型:
--
作者:
Abebe F;Belay M;Legesse M;K L M C F;Ottenhoff THM
As part of a major project to investigate protective and diagnostic immune markers against tuberculosis (TB), we measured antibody isotype responses to Mycobacterium tuberculosis (Mtb) antigens (LAM, Rv2031, and HBHA) in cohorts of 149 pulmonary tuberculosis patients (PTBP), 148 household contacts (HHCs), and 68 community controls (CCs) in an endemic setting. ELISA was used to measure levels of IgA, IgG, and IgM from sera of cohorts at baseline, and at 6 and 12 months from entry. The results show that there were significant differences in IgA, IgG, and IgM responses to the different antigens and in the three cohorts. At baseline, the level of IgM against RV2031 and LAM did not vary between cohorts, but the levels of IgA and IgG against Rv2031 were significantly higher in PTB patients than HHCs and CCs, followed by HHCs, and the lowest in CCs. In patients, there was a significant variation in antibody responses before and after chemotherapy. The levels of IgA and IgG against HBHA, and IgA against Rv2031 decreased significantly and remained low, while IgA and IgG against LAM increased significantly and remained high following chemotherapy. However, the levels of IgM against Rv2031 and LAM increased at 6 months but decreased again at 12 months. IgM against HBHA did not show any significant variation before and after chemotherapy. Similarly, there were also significant variations in antibody responses in HHCs over time. Our results show that there are significant variations in IgA, IgG and IgM responses to the different antigens and in the three cohorts, implying that not all antibody isotype responses are markers of clinical TB. In addition, the current and previous studies consistently show that IgA and IgG against Rv2031 discriminate between clinical disease, Mtb-infected and non-infected individuals.
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DOI:
10.4049/jimmunol.1601199
发表时间:
2017-03-01
期刊:
Journal of immunology (Baltimore, Md. : 1950)
影响因子:
--
作者:
Athman JJ;Sande OJ;Groft SG;Reba SM;Nagy N;Wearsch PA;Richardson ET;Rojas R;Boom WH;Shukla S;Harding CV
通讯作者:
Harding CV
影响因子:
3.7
作者:
Chegou NN;Essone PN;Loxton AG;Stanley K;Black GF;van der Spuy GD;van Helden PD;Franken KL;Parida SK;Klein MR;Kaufmann SH;Ottenhoff TH;Walzl G
通讯作者:
Walzl G
DOI:
10.1164/ajrccm.161.5.9908125
发表时间:
2000-05-01
影响因子:
24.7
作者:
Chan, ED;Reves, R;Hahn, WE
通讯作者:
Hahn, WE
影响因子:
3.1
作者:
CHAN, J;FAN, X;BLOOM, BR
通讯作者:
BLOOM, BR
DOI:
10.1073/pnas.1221708110
发表时间:
2013-05-28
影响因子:
11.1
作者:
Blattes, Emilyne;Vercellone, Alain;Puzo, Germain
通讯作者:
Puzo, Germain