Abstract
IT is now well established that congenital agammaglobulinæmia is associated with multiple serum protein deficiencies ; the sera of these patients lack 7S γ-globulins, 19S γ-globulins or β2M globulin, and β2A globulin1. Good et al.2,3 have recently reported that the sera of patients with agammaglobulinæmia contain three proteins not found in normal human sera and they have termed them β2K, β2E and γ1A globulins; their work was performed with antiserum from a horse immunized against human serum by Dr. P. Grabar. A review of our own immunoelectrophoretic patterns as well as those of Grabar et al. has failed to reveal any protein constituent other than C-reactive proteins in the sera of agammaglobulinæmic patients which is not ordinarily detectable in normal sera. Consequently the work reported here was undertaken to re-investigate this matter.
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References
Gitlin, D., in Analyse Immuno-Electrophorétique, edit. by Grabar, P., and Burtin, P. (Masson, Paris, 1960).
Bridges, R. A., and Good, R. A., Ann. N.Y. Acad. Sci., 86, 1089 (1960).
Good, R. A., Zak, S. J., Condie, R. M., and Bridges, R. A., Pediat. Clin. N. Amer., 7, 397 (1960).
Scheidegger, J. J., Intern. Arch. Allergy App. Immunol., 7, 103 (1955).
Heremans, J., Les Globulines Sériques du Systeme Gamma (Masson, Paris, 1960).
Giedion, A., and Scheidegger, J. J., Helvet. Paediat. Acta., 3, 241 (1957).
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ROSEN, F., JANEWAY, C. & GITLIN, D. Immunoelectrophoretic Examination of Agammaglobulinæmia. Nature 191, 1109–1110 (1961). https://doi.org/10.1038/1911109a0
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DOI: https://doi.org/10.1038/1911109a0
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