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Disease Info Card
Alloimmunization
Information about Alloimmunization: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Alloimmunization
Most recent studies have shown that Alloimmunization shares some biological mechanisms with anemia, anemia-sickle-cell, blood-group-incompatibility, decreased-immunologic-activity-[pe], edema, erythroblastosis-fetal, fetal-diseases, hemolysis-(disorder), hemolytic-disorder, hemorrhage, leukemia, malignant-neoplasms, neonatal-alloimmune-thrombocytopenia, pregnancy-complications-hematologic, purpura, refractoriness-to-platelet-transfusion, rh-isoimmunization, rheumatic-heart-disease, transfusion-reaction.
Among the many pathways, these few ones have gauged particular interests from scientists studying Alloimmunization, and have been seen in publications frequently: Cell Activation, Cell Proliferation, Coagulation, Complement-dependent Cytotoxicity, Cytolysis, Donor Selection, Hemostasis, Humoral Immune Response, Hypersensitivity, Immune Response, Localization, Mating, Pathogenesis, Phagocytosis, Platelet Activation, Platelet Aggregation, Secretion, Sensitization, Tolerance Induction, Transport
Quite a number of genes have been found to play important roles in Alloimmunization, such as ABO, CD4, EPO, FUZ, HLA-B, HLA-DRB4, HLA-E, HPSE, IL2, ITGA2, ITGA2B, NAAA, RHCE, RHD, RNF130, SCD, TNC. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.