When it's good to have MAITs.
When it's good to have MAITs.
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DOI:
10.1111/imcb.12402
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发表时间:
2020-11
影响因子:
4
通讯作者:
Corbett AJ
中科院分区:
文献类型:
--
作者:
Souter MN;McCluskey J;Corbett AJ
Tuberculosis (TB) is an old disease with an impressive history of persistent human affliction throughout time. Previous approaches to harness the immune response to Mycobacterium tuberculosis (M. tb), the causative agent of TB, have been largely ineffective at reducing the global burden of TB. Among the new cellular players in bacterial immunity are mucosalassociated invariant T (MAIT) cells. In a recent study published in Mucosal Immunology1, Sakai et al. examined the MAIT cell response to M. tb and tested pre-infection (vaccination) or post-infection (therapeutic) MAIT cell boosting regimens to enhance M. tb clearance in a mouse model. Surprisingly, the authors observed that the timing of the boosted MAIT cell response resulted in profoundly different outcomes for M. tb immunity.Historically, TB was commonly referred to as “consumption”, from the ancient Greek “Phthisis”, describing the nature of a characteristic “wasting disease”. Improvements in public health and later the emergence of effective antibiotics dramatically reduced the presence of “consumption” in the developed world. Despite these successes, M. tb infections remain the leading cause of mortality from an infectious agent. Moreover, M. tb is highly prevalent, infecting approximately one quarter of all humans, particularly in the developing world, where a further ten million diagnoses are made each year. The only vaccine approved for prevention of TB is Bacillus Calmette-Guérin (BCG), a live, attenuated preparation of Mycobacterium bovis which has variable efficacy in humans. Attempts to develop an alternative to the BCG vaccine have been met with criticism for lacking diversity and stagnant development pipelines2. It is clear that immunity to mycobacterial diseases, including TB, is still poorly understood. While drug therapy remains the gold standard treatment for TB, the emergence of drug-resistant M. tb has made it increasingly challenging to treat. Thus, renewed effort to resolve the remaining mysteries in our understanding of mycobacterial immunity, described in part for MAIT cells by Sakai et al., may lead us to more informed vaccine design and bring us a step closer to reducing the burden of M. tb infection globally.
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DOI:
10.1126/science.aax6624
发表时间:
2019-10-25
期刊:
Science (New York, N.Y.)
影响因子:
--
作者:
Constantinides MG;Link VM;Tamoutounour S;Wong AC;Perez-Chaparro PJ;Han SJ;Chen YE;Li K;Farhat S;Weckel A;Krishnamurthy SR;Vujkovic-Cvijin I;Linehan JL;Bouladoux N;Merrill ED;Roy S;Cua DJ;Adams EJ;Bhandoola A;Scharschmidt TC;Aubé J;Fischbach MA;Belkaid Y
通讯作者:
Belkaid Y
DOI:
10.1084/jem.20160637
发表时间:
2016-11-14
期刊:
The Journal of experimental medicine
影响因子:
--
作者:
Meierovics AI;Cowley SC
通讯作者:
Cowley SC
影响因子:
6.4
作者:
Katelaris, Anthea L.;Jackson, Charlotte;Abubakar, Ibrahim
通讯作者:
Abubakar, Ibrahim
影响因子:
9.8
作者:
Gold MC;Cerri S;Smyk-Pearson S;Cansler ME;Vogt TM;Delepine J;Winata E;Swarbrick GM;Chua WJ;Yu YY;Lantz O;Cook MS;Null MD;Jacoby DB;Harriff MJ;Lewinsohn DA;Hansen TH;Lewinsohn DM
通讯作者:
Lewinsohn DM
影响因子:
8
作者:
Sakai S;Kauffman KD;Oh S;Nelson CE;Barry CE 3rd;Barber DL
通讯作者:
Barber DL