专题：Immunodeficiency and Autoimmune Disorders

This cluster of papers focuses on the genetic basis and clinical manifestations of primary immunodeficiency disorders, including immune dysregulation, Th17 cell deficiency, common variable immunodeficiency, and defects in the interferon-? pathway. It also discusses the use of hematopoietic stem cell transplantation and immunoglobulin replacement therapy in the management of these disorders.
最新文献
Human inborn errors of immunity: 2024 update on the classification from the International Union of Immunological Societies Expert Committee

article Full Text OpenAlex

Exploring the prognostic role of complex karyotype in chronic lymphocytic leukaemia patients treated with venetoclax‐based regimens

article Full Text OpenAlex

5-Chloro-2′-deoxycytidine Induces a Distinctive High-Resolution Mutational Spectrum of Transition Mutations In Vivo

article Full Text OpenAlex

Pathogenic GATA2 genetic variants utilize an obligate enhancer mechanism to distort a multilineage differentiation program

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Case report: Rapidly progressive neurocognitive disorder with a fatal outcome in a patient with PU.1 mutated agammaglobulinemia

article Full Text OpenAlex

Uptake and safety of pneumococcal vaccination in adults with immune-mediated inflammatory diseases: a UK wide observational study

article Full Text OpenAlex

The Scope and Impact of Viral Infections in Common Variable Immunodeficiency (CVID) and CVID-like Disorders: A Literature Review

review Full Text OpenAlex

Pozelimab, a human monoclonal immunoglobulin for the treatment of CHAPLE disease

review Full Text OpenAlex

CNS Aspergillosis and Cryptococcosis with Cytomegalovirus Pneumonia in a Patient with Chronic Lymphocytic Leukemia Treated with Acalabrutinib

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Immunophenotypic variations in syphilis: insights from Mendelian randomization analysis

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近5年高被引文献
Human Inborn Errors of Immunity: 2022 Update on the Classification from the International Union of Immunological Societies Expert Committee

article Full Text OpenAlex 1037 FWCI122.81712126

The 2022 Update of IUIS Phenotypical Classification for Human Inborn Errors of Immunity

article Full Text OpenAlex 440 FWCI51.60680961

Pirtobrutinib in relapsed or refractory B-cell malignancies (BRUIN): a phase 1/2 study

article Full Text OpenAlex 418 FWCI64.86836977

X-linked recessive TLR7 deficiency in ~1% of men under 60 years old with life-threatening COVID-19

article Full Text OpenAlex 398 FWCI68.13775126

Zanubrutinib or Ibrutinib in Relapsed or Refractory Chronic Lymphocytic Leukemia

article Full Text OpenAlex 370 FWCI83.74072078

Bimekizumab versus Secukinumab in Plaque Psoriasis

article Full Text OpenAlex 348 FWCI27.35370517

Risankizumab as induction therapy for Crohn's disease: results from the phase 3 ADVANCE and MOTIVATE induction trials

article Full Text OpenAlex 338 FWCI86.13598705

Newer Biologic and Small-Molecule Therapies for Inflammatory Bowel Disease

review Full Text OpenAlex 305 FWCI43.06142054

Preexisting autoantibodies to type I IFNs underlie critical COVID-19 pneumonia in patients with APS-1

article Full Text OpenAlex 290 FWCI49.42702184

Antibodies to watch in 2021

review Full Text OpenAlex 285 FWCI28.40933476