Inborn errors of immunity(IEI)disorders,formerly primary immune deficiency diseases,are a heterogeneous group of disorders with variable hereditary transitions,clinical manifestations,complications and varying disease...
This work was supported by the COVID-19 Emergency Project of the National Key Research and Development Program of China(2022YFC0867900);the National Natural Science Foundation of China(32072944);the Emergency Scientific Research on Epidemic Prevention and Control of Henan Province(211100310200);Science and Technology Project of Henan Province(21210230180);Medical Science and Technology project of Henan Province(LHGJ20210274).
Dear Editor,Human immunodeficiency virus(HIV)is a lentivirus that,if left untreated,can lead to acquired immunodeficiency syndrome(AIDS).The virus can be divided into two types based on genetic differences:HIV-1 and H...
In the sentence beginning‘To trace cell proliferation,FO and MZ B cells’and the sentence beginning‘For cell activation,naïve B cells or CH12F3 cells’in this article,the[10 ng/ml]‘F(ab’)_(2)fragment goat anti-mou...
supported by a grant(1R01AI12140301A1)from the National Institutes of Health(NIH)in the USA.
Immunodeficiency,centromeric instability,and facial anomalies(ICF)syndrome is a rare autosomal recessive disorder characterized by DNA hypomethylation and antibody deficiency.It is caused by mutations in DNMT3B,ZBTB24...
supported by grants from the Start-up Foundation of Tsinghua University(No.400-53332101822);the Tsinghua-Peking Center for Life Sciences(No.045-61000100122);the National Key R&D Program of China(Nos.2021YFC2301900 and 2021YFC2301905);the National Natural Science Foundation of China(Nos.32200036 and 81974303);the Beijing Natural Science Foundation(Nos.L222068 and Z220018);the High-Level Public Health Specialized Talents Project of Beijing Municipal Health Commission(No.2022-2-018);the Beijing Key Laboratory for HIV/AIDS Research(No.BZ0089)
Over the past few years,the human virome and its complex interactions with microbial communities and the immune system have gained recognition as a crucial factor in human health.Individuals with compromised immune fu...
This work was supported by the National Key Research and Development Program of China(2021YFA0805300,2021YFA0805204);the National Natural Science Foundation of China(82171244,81922026,32170981);Guangzhou Key Research Program on Brain Science(202007030008).
Severe combined immunodeficiency(SCiD)encompasses a range of inherited disorders that lead to a profound deterioration of the immune system.Among the pivotal genes associated with SCID,RAG1 and IL2RG play crucial role...
supported by the VIB Grand Challenges Program,the KU Leuven C1 program,the European Union’s Horizon 2020 research and innovation program under grant agreement No 779295(to AL);the Biotechnology and Biological Sciences Research Council(BBSRC)through Institute Strategic Program Grant funding BBS/E/B/000C0427 and BBS/E/B/000C0428 and the KU Leuven BOFZAP start-up grant(to SH-B);Work in the Bultynck team was supported by grants from the Research Council of the KU Leuven(C14/19/99 and AKUL/19/34);Research Foundation-Flanders(G.0818.21N;G.0945.22N);DIY is supported by the National Institutes of Health(NIH)R01-DE0014756 grant.MRB and IIS are supported by the NIH R01GM072804 grant(to IIS);the Welch Foundation Research Grant AU-2014-20190331(to IIS);the American Heart Association grant 18CDA34110086(to MRB);IIS,DIY,and GB are in the FWO Scientific Research Network CaSign(W0.019.17N);IM and RS are FWO senior clinical investigator fellows.IM and RS are members of the European Reference Network for Rare Immunodeficiency,Autoinflammatory and Autoimmune Diseases(project ID No.739543).
Calcium signaling is essential for lymphocyte activation, with genetic disruptions of store-operated calcium (Ca^(2+)) entry resulting in severe immunodeficiency. The inositol 1,4,5-trisphosphate receptor (IP_(3)R), a...
In this article the statement in the Acknowledgements section was incorrectly given as “MRB and IIS are supported by the NIH R01GM080139 grant (to IIS), the Welch Foundation Research Grant AU-2014-20190331 (to IIS), ...
Background:The DNA-repair enzyme Artemis is essential for rearrangement of T-and B-cell receptors.Mutations in DCLRE1C,which encodes Artemis,cause Artemis-deficient severe combined immunodeficiency(ART-SCID),which is ...
supported by the National Natural Science Foundation of China(31970839);the National Key R&D Program of China(1316203);Independent Innovation Research Fund of Huazhong University of Science and Technology(2020kfyXGYJ017);the HUST Academic Frontier Youth Team(2018QYTD10).
The SARS-CoV-2 infection causes severe immune disruption.However,it is unclear if disrupted immune regulation still exists and pertains in recovered COVID-19 patients.In our study,we have characterized the immunephe n...