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  2. X-linked agammaglobulinemia - Wikipedia

    en.wikipedia.org/wiki/X-linked_agammaglobulinemia

    X-chromosome. Most antibodies are gamma globulins. Antibodies are made mainly by plasma cells, which are daughter cells of the B cell line.The Btk enzyme plays an essential role in the maturation of B cells in the bone marrow, and when mutated, immature pro-B lymphocytes are unable to develop into pre-B lymphocytes, which normally develop into mature (naive) B cells that leave the bone marrow ...

  3. Bruton's tyrosine kinase - Wikipedia

    en.wikipedia.org/wiki/Bruton's_tyrosine_kinase

    Bruton's tyrosine kinase is named for Ogden Bruton, who first described XLA in 1952. [10] [40] Later studies in 1993 and 1994 reported the discovery of BTK (initially termed B cell progenitor kinase or BPK) and found that BTK levels are reduced in B cells from XLA patients. [41] [42] [43]

  4. Ogden Bruton - Wikipedia

    en.wikipedia.org/wiki/Ogden_Bruton

    While at Walter Reed during his second tour, Bruton studied an 8-year-old boy, Joseph S. Holtoner, Jr., who had recurrent pneumonia infections and who lacked gamma globulin in his serum. This type of agammaglobulinemia is now called Bruton's syndrome or X-linked agammaglobulinemia, which was later found by others to be an X-linked congenital ...

  5. Gamma globulin - Wikipedia

    en.wikipedia.org/wiki/Gamma_globulin

    Intravenous gamma globulin was FDA-approved in 2004 to reduce antibodies in a patient with kidney failure to allow that person to accept a kidney from a donor with a different blood type (ABO-incompatible), or who is an unacceptable tissue match. Stanley Jordan at Cedars-Sinai Medical Center in Los Angeles pioneered this treatment. [4]

  6. Severe combined immunodeficiency - Wikipedia

    en.wikipedia.org/wiki/Severe_combined...

    Severe combined immunodeficiency (SCID), also known as Swiss-type agammaglobulinemia, is a rare genetic disorder characterized by the disturbed development of functional T cells and B cells caused by numerous genetic mutations that result in differing clinical presentations. [2]

  7. Ibrutinib - Wikipedia

    en.wikipedia.org/wiki/Ibrutinib

    Ibrutinib is a potent, irreversible inhibitor of Bruton's tyrosine kinase (BTK). The acrylamide group of ibrutinib forms a covalent bond with the cysteine residue C481 in the BTK active site, leading to sustained inhibition of BTK enzymatic activity. BTK is an important signalling molecule of the B-cell antigen receptor (BCR) pathway, which ...

  8. Review links 3 potentially-blinding eye conditions to GLP-1 ...

    www.aol.com/lifestyle/review-links-3-potentially...

    A new review reports that nine people taking semaglutide and tirzepatide — the active ingredient in GLP-1 medications — experienced vision issues, including three potentially blinding eye ...

  9. Dysgammaglobulinemia - Wikipedia

    en.wikipedia.org/wiki/Dysgammaglobulinemia

    Dysgammaglobulinemia is a type of immune disorder characterized by a reduction in some types of gamma globulins, resulting in heightened susceptibility to some infectious diseases where primary immunity is antibody based.