Therapeutic potential for blockade of the CD40 ligand, gp39
Author:
Publisher
Springer Science and Business Media LLC
Subject
Immunology,Immunology and Allergy
Link
http://link.springer.com/content/pdf/10.1007/BF01540954.pdf
Reference56 articles.
1. Foy TM, Aruffo A, Ledbetter JA, Noelle RJ: In vivo CD40-gp39 interactions are essential for thymus-dependent immunity. II. Prolonged in vivo suppression of primary and secondary humoral immune responses by an antibody targeted to the CD40 ligand, gp39. J Exp Med 178:1567?1575, 1993
2. Van den Eertwegh AJM, Noelle RJ, Roy M, Shepherd DM, Aruffo A, Ledbetter JA, Boersma WJA, Claassen E:In vivo CD40-gp39 interactions are essential for thymus-dependent immunity. I. CD40-gp39 interactions are essential for thymus dependent humoral immunity and identify sites of cognate interactions in vivo. J Exp Med 178:1555?1565, 1993
3. Foy TM, Laman JD, Ledbetter JA, Aruffo A, Claassen E, Noelle RJ: gp39-CD40 interactions are essential for germinal center formation and the development of B cell memory. J Exp Med 180:157?164, 1994
4. Gray D, Siepmann K, Wohlleben G: CD40 ligation in B cell activation, isotype switching and memory development. Semin Immunol 6:303?310, 1994
5. Allen RC, Armitage RJ, Conley ME, Rosenblatt H, Jenkins NA, Copeland NG, Bedell MA, Edelhoff S, Disteche J, Simoneaux DK, Fanslow WC, Belmont J, Spriggs MK: CD40 ligand gene defects responsible for X-linked hyper-IgM Syndrome. Science 259:990?993, 1993
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