1Futei Y, Amagai M, Ishii K, et al. Predominant IgG4 subclass in autoantibodies of pemphigus vulgaris and foliaceus[J]. J Dermatol Sci, 2001,26:55-61.
2Grey H M, Kunkel H G. H chain subgroups of myeloma ang normal 7s gamma-globulin[J]. J Exp Med,1964,120: 253-266.
3Spiegelberg H I. Biological activities of different classes and subclasses[J]. Adv Immunol, 1974, 19: 259-294.
4Van der Zee J S, van Swielen P, Aaleherse R C. Inhibition of complement activation by IgG4 antibodies[J]. Clin Exp Immunol, 1986, 64 (2):415-422.
5Neild G H, Rodriguez Justo M, Mall C, et al. Systemic extrapancreatic lesions associated with autoimmune pancreatitis[J]. BMC Med,2005,31:232-237.
6Yoshida K, Toki F, Takeu chi T, et al. Chronic pancreatitis caused by an autoimmune abnormality. Proposal of the concept of autoimmune pancreatitis[J]. Dig Dis Sci,1995,40(7):1561- 1568.
7Kamisawa T, Funata N, Hayashi Y, et al. A new clinicopatho-logical entity of IgG4-related autoimmune disease[J]. J Gastroenterol, 2003, 38(10):982-984.
8Geyer J T, Ferry J A, Harris N L, et al. Chronic sclerosing sialadenitis (kuttner tumor ) is an IgG4-associated disease[J]. Am J Surg Pathol, 2010, 34(2):202-210.
9Tabata T, Kamisawa T, Takuma K, et al. Serial changes of elevated serum IgG4 leves in IgG4-related systemic disease [J]. Intern Med ,2011, 50(2):69-75.
10Okazaki K, Umehara H. Are classification criteria for IgG4-RD now possible? The concept of IgG4-related disease and proposal of comprehensive diagnostic criteria in Japan[J]. Int J eumatol. 2012. 12 : 357-371.
