Skip to main content
Erschienen in: Modern Rheumatology 3/2012

01.06.2012 | Original Article

Value of serum IgG4 in the diagnosis of IgG4-related disease and in differentiation from rheumatic diseases and other diseases

verfasst von: Motohisa Yamamoto, Tetsuya Tabeya, Yasuyoshi Naishiro, Hidetaka Yajima, Keisuke Ishigami, Yui Shimizu, Mikiko Obara, Chisako Suzuki, Kentaro Yamashita, Hiroyuki Yamamoto, Toshiaki Hayashi, Shigeru Sasaki, Toshiaki Sugaya, Tadao Ishida, Ken-ichi Takano, Tetsuo Himi, Yasuo Suzuki, Norihiro Nishimoto, Saho Honda, Hiroki Takahashi, Kohzoh Imai, Yasuhisa Shinomura

Erschienen in: Modern Rheumatology | Ausgabe 3/2012

Einloggen, um Zugang zu erhalten

Abstract

IgG4-related disease (IgG4-RD) is a novel disease entity that includes Mikulicz’s disease, autoimmune pancreatitis (AIP), and many other conditions. It is characterized by elevated serum IgG4 levels and abundant IgG4-bearing plasmacyte infiltration of involved organs. We postulated that high levels of serum IgG4 would comprise a useful diagnostic tool, but little information is available about IgG4 in conditions other than IgG4-RD, including rheumatic diseases. Several reports have described cutoff values for serum IgG4 when diagnosing IgG4-RD, but these studies mostly used 135 mg/dL in AIP to differentiate from pancreatic cancer instead of rheumatic and other common diseases. There is no evidence for a cutoff serum IgG4 level of 135 mg/dL for rheumatic diseases and common diseases that are often complicated with rheumatic diseases. The aim of this work was to re-evaluate the usual cutoff serum IgG4 value in AIP (135 mg/dL) that is used to diagnose whole IgG4-RD in the setting of a rheumatic clinic by measuring serum IgG4 levels in IgG4-RD and various disorders. We therefore constructed ROC curves of serum IgG4 levels in 418 patients who attended Sapporo Medical University Hospital due to IgG4-RD and various rheumatic and common disorders. The optimal cut-off value of serum IgG4 for a diagnosis of IgG4-RD was 144 mg/dL, and the sensitivity and specificity were 95.10 and 90.76%, respectively. Levels of serum IgG4 were elevated in IgG4-RD, Churg–Strauss syndrome, multicentric Castleman’s disease, eosinophilic disorders, and in some patients with rheumatoid arthritis, systemic sclerosis, chronic hepatitis, and liver cirrhosis. The usual cut-off value of 135 mg/dL in AIP is useful for diagnosing whole IgG4-RD, but high levels of serum IgG4 are sometimes observed in not only IgG4-RD but also other rheumatic and common diseases.
Literatur
1.
Zurück zum Zitat Ghazale A, Chari ST, Smyrk TC, et al. Value of serum IgG4 in the diagnosis of autoimmune pancreatitis and in distinguishing it from pancreatic cancer. Am J Gastroenterol. 2007;102:1646–53.PubMedCrossRef Ghazale A, Chari ST, Smyrk TC, et al. Value of serum IgG4 in the diagnosis of autoimmune pancreatitis and in distinguishing it from pancreatic cancer. Am J Gastroenterol. 2007;102:1646–53.PubMedCrossRef
2.
Zurück zum Zitat Choi EK, Kim MH, Lee TY, et al. The sensitivity and specificity of serum immunoglobulin G and immunoglobulin G4 levels in the diagnosis of autoimmune chronic pancreatitis: Korean experience. Pancreas. 2007;35:156–61.PubMedCrossRef Choi EK, Kim MH, Lee TY, et al. The sensitivity and specificity of serum immunoglobulin G and immunoglobulin G4 levels in the diagnosis of autoimmune chronic pancreatitis: Korean experience. Pancreas. 2007;35:156–61.PubMedCrossRef
3.
Zurück zum Zitat Morselli-Labate AM, Pezzilli R. Usefulness of serum IgG4 in the diagnosis and follow up of autoimmune pancreatitis: a systematic literature review and meta-analysis. J Gastroenterol Hepatol. 2009;24:15–36.PubMedCrossRef Morselli-Labate AM, Pezzilli R. Usefulness of serum IgG4 in the diagnosis and follow up of autoimmune pancreatitis: a systematic literature review and meta-analysis. J Gastroenterol Hepatol. 2009;24:15–36.PubMedCrossRef
4.
Zurück zum Zitat Song TJ, Kim MH, Moon SH, et al. The combined measurement of total serum IgG and IgG4 may increase diagnostic sensitivity for autoimmune pancreatitis without sacrificing sensitivity, compared with IgG4 alone. Am J Gastroenterol. 2010;105:1655–60.PubMedCrossRef Song TJ, Kim MH, Moon SH, et al. The combined measurement of total serum IgG and IgG4 may increase diagnostic sensitivity for autoimmune pancreatitis without sacrificing sensitivity, compared with IgG4 alone. Am J Gastroenterol. 2010;105:1655–60.PubMedCrossRef
5.
Zurück zum Zitat Sadler R, Chapman RW, Simpson D, et al. The diagnostic significance of serum IgG4 levels in patients with autoimmune pancreatitis: a UK study. Eur J Gastroenterol Hepatol. 2011;23:139–45.PubMedCrossRef Sadler R, Chapman RW, Simpson D, et al. The diagnostic significance of serum IgG4 levels in patients with autoimmune pancreatitis: a UK study. Eur J Gastroenterol Hepatol. 2011;23:139–45.PubMedCrossRef
6.
Zurück zum Zitat Okazaki K, Kawa S, Kamisawa T, et al. Clinical diagnostic criteria of autoimmune pancreatitis: revised proposal. J Gastroenterol. 2006;41:626–31.PubMedCrossRef Okazaki K, Kawa S, Kamisawa T, et al. Clinical diagnostic criteria of autoimmune pancreatitis: revised proposal. J Gastroenterol. 2006;41:626–31.PubMedCrossRef
7.
Zurück zum Zitat Chari ST, Smyrk TC, Levy MJ, et al. Diagnosis of autoimmune pancreatitis: the Mayo Clinic experience. Clin Gastroenterol Hepatol. 2006;4:1010–6.PubMedCrossRef Chari ST, Smyrk TC, Levy MJ, et al. Diagnosis of autoimmune pancreatitis: the Mayo Clinic experience. Clin Gastroenterol Hepatol. 2006;4:1010–6.PubMedCrossRef
8.
Zurück zum Zitat Hochberg MC. Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum. 1997;40:1725.PubMedCrossRef Hochberg MC. Updating the American College of Rheumatology revised criteria for the classification of systemic lupus erythematosus. Arthritis Rheum. 1997;40:1725.PubMedCrossRef
9.
Zurück zum Zitat Miyakis S, Lockshin MD, Atsumi T, et al. International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS). J Thromb Haemost. 2006;4:295–306.PubMedCrossRef Miyakis S, Lockshin MD, Atsumi T, et al. International consensus statement on an update of the classification criteria for definite antiphospholipid syndrome (APS). J Thromb Haemost. 2006;4:295–306.PubMedCrossRef
10.
Zurück zum Zitat Aletaha D, Neogi T, Silman AJ, et al. 2010 Rheumatoid arthritis classification criteria: an American College of Rheumatology/European League Against Rheumatism collaborative initiative. Arthritis Rheum. 2010;62:2569–81.PubMedCrossRef Aletaha D, Neogi T, Silman AJ, et al. 2010 Rheumatoid arthritis classification criteria: an American College of Rheumatology/European League Against Rheumatism collaborative initiative. Arthritis Rheum. 2010;62:2569–81.PubMedCrossRef
11.
Zurück zum Zitat Subcommittee for Scleroderma Criteria of the American Rheumatism Association Diagnostic and Therapeutic Criteria Committee. Preliminary criteria for the classification of systemic sclerosis (scleroderma). Arthritis Rheum. 1980;23:581–90. Subcommittee for Scleroderma Criteria of the American Rheumatism Association Diagnostic and Therapeutic Criteria Committee. Preliminary criteria for the classification of systemic sclerosis (scleroderma). Arthritis Rheum. 1980;23:581–90.
12.
Zurück zum Zitat Bohan A, Peter JB, Bowman RL, et al. A computer-assisted analysis of 153 patients with polymyositis and dermatomyositis. Medicine (Baltimore). 1977;56:255–86. Bohan A, Peter JB, Bowman RL, et al. A computer-assisted analysis of 153 patients with polymyositis and dermatomyositis. Medicine (Baltimore). 1977;56:255–86.
13.
Zurück zum Zitat Alarcon-Segovia D, Cardiel MH. Comparison between 3 diagnostic criteria for mixed connective tissue disease: study of 593 patients. J Rheumatol. 1989;16:328–34.PubMed Alarcon-Segovia D, Cardiel MH. Comparison between 3 diagnostic criteria for mixed connective tissue disease: study of 593 patients. J Rheumatol. 1989;16:328–34.PubMed
14.
Zurück zum Zitat Vitali C, Bombardieri S, Jonsson R, et al. Classification criteria for Sjögren’s syndrome: a revised version of the European criteria proposed by the American-European Consensus Group. Ann Rheum Dis. 2002;61:554–8.PubMedCrossRef Vitali C, Bombardieri S, Jonsson R, et al. Classification criteria for Sjögren’s syndrome: a revised version of the European criteria proposed by the American-European Consensus Group. Ann Rheum Dis. 2002;61:554–8.PubMedCrossRef
15.
Zurück zum Zitat International Study Group for Behçet’s Disease. Evaluation of diagnostic (“classification”) criteria in Behçet’s disease—towards internationally agreed criteria. Br J Rheumatol. 1992;31:299–308. International Study Group for Behçet’s Disease. Evaluation of diagnostic (“classification”) criteria in Behçet’s disease—towards internationally agreed criteria. Br J Rheumatol. 1992;31:299–308.
16.
Zurück zum Zitat Guillevin L, Durand-Gasselin B, Cevallos R, et al. Microscopic polyangiitis: clinical and laboratory findings in eighty-five patients. Arthritis Rheum. 1999;42:421–30.PubMedCrossRef Guillevin L, Durand-Gasselin B, Cevallos R, et al. Microscopic polyangiitis: clinical and laboratory findings in eighty-five patients. Arthritis Rheum. 1999;42:421–30.PubMedCrossRef
17.
Zurück zum Zitat Masi AT, Hunder GG, Lie JT, et al. The American College of Rheumatology 1990 criteria for the classification of Churg–Strauss syndrome (allergic granulomatosis and angiitis). Arthritis Rheum. 1990;33:1094–100.PubMedCrossRef Masi AT, Hunder GG, Lie JT, et al. The American College of Rheumatology 1990 criteria for the classification of Churg–Strauss syndrome (allergic granulomatosis and angiitis). Arthritis Rheum. 1990;33:1094–100.PubMedCrossRef
18.
Zurück zum Zitat van Gestel AM, Prevoo ML, van’t Hof MA, van Rijswijk MH, van de Putte LB, van Riel PL. Development and validation of the European League Against Rheumatism response criteria for rheumatoid arthritis. Comparison with the preliminary American College of Rheumatology and the World Health Organization/International League Against Rheumatism Criteria. Arthritis Rheum. 1996;39:34–40.PubMedCrossRef van Gestel AM, Prevoo ML, van’t Hof MA, van Rijswijk MH, van de Putte LB, van Riel PL. Development and validation of the European League Against Rheumatism response criteria for rheumatoid arthritis. Comparison with the preliminary American College of Rheumatology and the World Health Organization/International League Against Rheumatism Criteria. Arthritis Rheum. 1996;39:34–40.PubMedCrossRef
19.
Zurück zum Zitat Clements PJ, Lachenbruch PA, Seibold JR, et al. Inter and intraobserver variability of total skin thickness score (modified Rodnan TSS) in systemic sclerosis. J Rheum. 1995;22:1281–5.PubMed Clements PJ, Lachenbruch PA, Seibold JR, et al. Inter and intraobserver variability of total skin thickness score (modified Rodnan TSS) in systemic sclerosis. J Rheum. 1995;22:1281–5.PubMed
20.
Zurück zum Zitat Hamano H, Kawa S, Horiuchi A, et al. High serum IgG4 concentrations in patients with sclerosing pancreatitis. N Engl J Med. 2001;344:732–8.PubMedCrossRef Hamano H, Kawa S, Horiuchi A, et al. High serum IgG4 concentrations in patients with sclerosing pancreatitis. N Engl J Med. 2001;344:732–8.PubMedCrossRef
21.
Zurück zum Zitat Yamamoto M, Harada S, Ohara M, et al. Clinical and pathological differences between Mikulicz’s disease and Sjögren’s syndrome. Rheumatology (Oxf). 2005;44:227–34. Yamamoto M, Harada S, Ohara M, et al. Clinical and pathological differences between Mikulicz’s disease and Sjögren’s syndrome. Rheumatology (Oxf). 2005;44:227–34.
22.
Zurück zum Zitat van der Giessen M, Rossouw E, van Teen TA. Quantification of IgG subclasses in sera of normal adults and healthy children between 4 and 12 years of age. Clin Exp Immunol. 1975;21:501–9.PubMed van der Giessen M, Rossouw E, van Teen TA. Quantification of IgG subclasses in sera of normal adults and healthy children between 4 and 12 years of age. Clin Exp Immunol. 1975;21:501–9.PubMed
23.
Zurück zum Zitat Schur PH, Rosen F, Norman ME. Immunoglobulin subclasses in normal children. Pediatr Res. 1979;13:181–3.PubMedCrossRef Schur PH, Rosen F, Norman ME. Immunoglobulin subclasses in normal children. Pediatr Res. 1979;13:181–3.PubMedCrossRef
24.
Zurück zum Zitat Schauer U, Stemberg F, Rieger CH, et al. IgG subclass concentration in certified reference material 470 and reference values for children and adults determined with the binding site reagents. Clin Chem. 2003;49:1924–9.PubMedCrossRef Schauer U, Stemberg F, Rieger CH, et al. IgG subclass concentration in certified reference material 470 and reference values for children and adults determined with the binding site reagents. Clin Chem. 2003;49:1924–9.PubMedCrossRef
25.
Zurück zum Zitat Leddy JP, Deitchman J, Bakemeier RF. IgG subclasses measurement of radioimmunoassay in normal and hypogammaglobulinaemic sera. Arthritis Rheum. 1970;13:331–2. Leddy JP, Deitchman J, Bakemeier RF. IgG subclasses measurement of radioimmunoassay in normal and hypogammaglobulinaemic sera. Arthritis Rheum. 1970;13:331–2.
26.
Zurück zum Zitat Morell A, Skavaril F. A modified radioimmunoassay for quantitative determination of IgG subclasses in man. Prot Biol Fluids. 1971;19:533–40. Morell A, Skavaril F. A modified radioimmunoassay for quantitative determination of IgG subclasses in man. Prot Biol Fluids. 1971;19:533–40.
27.
Zurück zum Zitat Shakib F, Stanworth DR, Drew R, et al. A quantitative study of the distribution of IgG sub-classes in a group of normal human sera. J Immunol Methods. 1975;8:17–28.PubMedCrossRef Shakib F, Stanworth DR, Drew R, et al. A quantitative study of the distribution of IgG sub-classes in a group of normal human sera. J Immunol Methods. 1975;8:17–28.PubMedCrossRef
28.
Zurück zum Zitat Oxelius V. Crossed immunoelectrophoresis and electroimmunoassay of human IgG subclass. Acta Path Microbiol Scand Sect C. 1978;86:109–18. Oxelius V. Crossed immunoelectrophoresis and electroimmunoassay of human IgG subclass. Acta Path Microbiol Scand Sect C. 1978;86:109–18.
29.
Zurück zum Zitat French MAH, Harrison G. Serum IgG subclass concentration in healthy adults: a study using monoclonal antisera. Clin Exp Immnol. 1984;56:473–5. French MAH, Harrison G. Serum IgG subclass concentration in healthy adults: a study using monoclonal antisera. Clin Exp Immnol. 1984;56:473–5.
30.
Zurück zum Zitat Milford-Ward A, White PAE, French MAH, et al. A calibration material for IgG subclass assay. J Clin Lab Immunol. 1984;14:209–10.PubMed Milford-Ward A, White PAE, French MAH, et al. A calibration material for IgG subclass assay. J Clin Lab Immunol. 1984;14:209–10.PubMed
31.
Zurück zum Zitat Klein F, Skvaril F, Vermeeren R, et al. The quantification of human IgG subclasses in reference preparations. Clin Chim Acta. 1985;150:119–27.PubMedCrossRef Klein F, Skvaril F, Vermeeren R, et al. The quantification of human IgG subclasses in reference preparations. Clin Chim Acta. 1985;150:119–27.PubMedCrossRef
32.
Zurück zum Zitat Maddessery JV, Kwon OH, Lee SY, et al. IgG2 subclass deficiency: IgG subclass assay and IgG2 concentrations among 8015 blood donors. Clin Chem. 1988;34:1407–13. Maddessery JV, Kwon OH, Lee SY, et al. IgG2 subclass deficiency: IgG subclass assay and IgG2 concentrations among 8015 blood donors. Clin Chem. 1988;34:1407–13.
33.
Zurück zum Zitat Carr-Smith HD, Overton J, Bradwell AR. IgG subclass value assignment to the protein reference preparation CRM 470. Clin Chem. 1997;43(Suppl 6):S238. Carr-Smith HD, Overton J, Bradwell AR. IgG subclass value assignment to the protein reference preparation CRM 470. Clin Chem. 1997;43(Suppl 6):S238.
34.
Zurück zum Zitat Yamamoto M, Ohara M, Suzuki C, et al. Elevated IgG4 concentrations in serum of patients with Mikulicz’s disease. Scand J Rheumatol. 2004;33:432–3.PubMedCrossRef Yamamoto M, Ohara M, Suzuki C, et al. Elevated IgG4 concentrations in serum of patients with Mikulicz’s disease. Scand J Rheumatol. 2004;33:432–3.PubMedCrossRef
35.
Zurück zum Zitat Yamamoto M, Takahashi H, Suzuki C, et al. Analysis of serum IgG subclasses in Churg–Strauss syndrome—the meaning of elevated serum levels of IgG4. Intern Med. 2010;49:1365–70.PubMedCrossRef Yamamoto M, Takahashi H, Suzuki C, et al. Analysis of serum IgG subclasses in Churg–Strauss syndrome—the meaning of elevated serum levels of IgG4. Intern Med. 2010;49:1365–70.PubMedCrossRef
36.
Zurück zum Zitat Yamamoto M, Takahashi H, Suzuki C, et al. The analysis of interleukin-6 in patients with systemic IgG4-related plasmacytic syndrome (SIPS)—expansion of SIPS to the territory of Castleman’s disease. Rheumatology (Oxf). 2009;48:860–2.CrossRef Yamamoto M, Takahashi H, Suzuki C, et al. The analysis of interleukin-6 in patients with systemic IgG4-related plasmacytic syndrome (SIPS)—expansion of SIPS to the territory of Castleman’s disease. Rheumatology (Oxf). 2009;48:860–2.CrossRef
37.
Zurück zum Zitat Shinoda K, Matsui S, Taki H, et al. Deforming arthropathy in a patient with IgG4-related systemic disease: comment on the article by Stone et al. Arthritis Care Res (Hoboken). 2011;63:172.CrossRef Shinoda K, Matsui S, Taki H, et al. Deforming arthropathy in a patient with IgG4-related systemic disease: comment on the article by Stone et al. Arthritis Care Res (Hoboken). 2011;63:172.CrossRef
38.
Zurück zum Zitat Engelmann R, Brandt J, Eggert M, et al. IgG1 and IgG4 are the predominant subclasses among auto-antibodies against two citrullinated antigens in RA. Rheumatology (Oxf). 2008;47:1489–92.CrossRef Engelmann R, Brandt J, Eggert M, et al. IgG1 and IgG4 are the predominant subclasses among auto-antibodies against two citrullinated antigens in RA. Rheumatology (Oxf). 2008;47:1489–92.CrossRef
39.
Zurück zum Zitat Bos WH, Bartelds GM, Vis M, et al. Preferential decrease in IgG4 anti-citrullinated protein antibodies during treatment with tumour necrosis factor blocking agents in patients with rheumatoid arthritis. Ann Rheum Dis. 2009;68:558–63.PubMedCrossRef Bos WH, Bartelds GM, Vis M, et al. Preferential decrease in IgG4 anti-citrullinated protein antibodies during treatment with tumour necrosis factor blocking agents in patients with rheumatoid arthritis. Ann Rheum Dis. 2009;68:558–63.PubMedCrossRef
40.
Zurück zum Zitat Wang W, Li J. Identification of natural bispecific antibodies against cyclic citrullinated peptide and immunoglobulin G in rheumatoid arthritis. PLoS One. 2011;6:e16527.PubMedCrossRef Wang W, Li J. Identification of natural bispecific antibodies against cyclic citrullinated peptide and immunoglobulin G in rheumatoid arthritis. PLoS One. 2011;6:e16527.PubMedCrossRef
41.
Zurück zum Zitat Kuwana M, Okano Y, Pandey JP, et al. Enzyme-linked immunosorbent assay for detection of anti-RNA polymerase III antibody: analytical accuracy and clinical associations in systemic sclerosis. Arthritis Rheum. 2005;52:2425–32.PubMedCrossRef Kuwana M, Okano Y, Pandey JP, et al. Enzyme-linked immunosorbent assay for detection of anti-RNA polymerase III antibody: analytical accuracy and clinical associations in systemic sclerosis. Arthritis Rheum. 2005;52:2425–32.PubMedCrossRef
42.
Zurück zum Zitat Okazaki K, Uchida K, Koyabu M, Miyoshi H, Takaoka M. Recent advances in the concept and diagnosis of autoimmune pancreatitis and IgG4-related disease. J Gastroenterol. 2011;46:277–88.PubMedCrossRef Okazaki K, Uchida K, Koyabu M, Miyoshi H, Takaoka M. Recent advances in the concept and diagnosis of autoimmune pancreatitis and IgG4-related disease. J Gastroenterol. 2011;46:277–88.PubMedCrossRef
43.
Zurück zum Zitat Hummelshoj L, Ryder LP, Poulsen LK. The role of the interleukin-10 subfamily members in immunoglobulin production by human B cells. Scand J Immunol. 2006;64:40–7.PubMedCrossRef Hummelshoj L, Ryder LP, Poulsen LK. The role of the interleukin-10 subfamily members in immunoglobulin production by human B cells. Scand J Immunol. 2006;64:40–7.PubMedCrossRef
44.
Zurück zum Zitat Zen Y, Nakanuma Y. Pathogenesis of IgG4-related disease. Curr Opin Rheumatol. 2011;23:114–8.PubMedCrossRef Zen Y, Nakanuma Y. Pathogenesis of IgG4-related disease. Curr Opin Rheumatol. 2011;23:114–8.PubMedCrossRef
45.
Zurück zum Zitat Slobodin G, Ahmad MS, Rosner I, et al. Regulatory T cells (CD4(+)CD25(bright)FoxP3(+)) expansion in systemic sclerosis correlates with disease activity and severity. Cell Immunol. 2010;261:77–80.PubMedCrossRef Slobodin G, Ahmad MS, Rosner I, et al. Regulatory T cells (CD4(+)CD25(bright)FoxP3(+)) expansion in systemic sclerosis correlates with disease activity and severity. Cell Immunol. 2010;261:77–80.PubMedCrossRef
46.
Zurück zum Zitat Sato S, Hasegawa M, Takehara K. Serum levels of interleukin-6 and interleukin-10 correlate with total skin thickness score in patients with systemic sclerosis. J Dermatol Sci. 2001;27:140–6.PubMedCrossRef Sato S, Hasegawa M, Takehara K. Serum levels of interleukin-6 and interleukin-10 correlate with total skin thickness score in patients with systemic sclerosis. J Dermatol Sci. 2001;27:140–6.PubMedCrossRef
47.
Zurück zum Zitat Kirmaz C, Terzioglu E, Topalak O, et al. Serum transforming growth factor-β1 (TGF-β1) in patients with cirrhosis, chronic hepatitis B and chronic hepatitis C. Eur Cytokine Netw. 2004;15:112–6.PubMed Kirmaz C, Terzioglu E, Topalak O, et al. Serum transforming growth factor-β1 (TGF-β1) in patients with cirrhosis, chronic hepatitis B and chronic hepatitis C. Eur Cytokine Netw. 2004;15:112–6.PubMed
48.
Zurück zum Zitat Verma V, Chakravarti A, Kar P. Cytokine levels of TGF-beta, IL-10, and sTNFαRII in type C chronic liver disease. Dig Dis Sci. 2008;53:2233–7.PubMedCrossRef Verma V, Chakravarti A, Kar P. Cytokine levels of TGF-beta, IL-10, and sTNFαRII in type C chronic liver disease. Dig Dis Sci. 2008;53:2233–7.PubMedCrossRef
49.
Zurück zum Zitat Ishida C, Ikebuchi Y, Okamoto K, Murawaki Y. Functional gene polymorphisms of interleukin-10 are associated with liver disease progression in Japanese patients with hepatitis C virus infection. Intern Med. 2011;50:659–66.PubMedCrossRef Ishida C, Ikebuchi Y, Okamoto K, Murawaki Y. Functional gene polymorphisms of interleukin-10 are associated with liver disease progression in Japanese patients with hepatitis C virus infection. Intern Med. 2011;50:659–66.PubMedCrossRef
Metadaten
Titel
Value of serum IgG4 in the diagnosis of IgG4-related disease and in differentiation from rheumatic diseases and other diseases
verfasst von
Motohisa Yamamoto
Tetsuya Tabeya
Yasuyoshi Naishiro
Hidetaka Yajima
Keisuke Ishigami
Yui Shimizu
Mikiko Obara
Chisako Suzuki
Kentaro Yamashita
Hiroyuki Yamamoto
Toshiaki Hayashi
Shigeru Sasaki
Toshiaki Sugaya
Tadao Ishida
Ken-ichi Takano
Tetsuo Himi
Yasuo Suzuki
Norihiro Nishimoto
Saho Honda
Hiroki Takahashi
Kohzoh Imai
Yasuhisa Shinomura
Publikationsdatum
01.06.2012
Verlag
Springer Japan
Erschienen in
Modern Rheumatology / Ausgabe 3/2012
Print ISSN: 1439-7595
Elektronische ISSN: 1439-7609
DOI
https://doi.org/10.1007/s10165-011-0532-6

Weitere Artikel der Ausgabe 3/2012

Modern Rheumatology 3/2012 Zur Ausgabe

Leitlinien kompakt für die Innere Medizin

Mit medbee Pocketcards sicher entscheiden.

Seit 2022 gehört die medbee GmbH zum Springer Medizin Verlag

Erhebliches Risiko für Kehlkopfkrebs bei mäßiger Dysplasie

29.05.2024 Larynxkarzinom Nachrichten

Fast ein Viertel der Personen mit mäßig dysplastischen Stimmlippenläsionen entwickelt einen Kehlkopftumor. Solche Personen benötigen daher eine besonders enge ärztliche Überwachung.

Nach Herzinfarkt mit Typ-1-Diabetes schlechtere Karten als mit Typ 2?

29.05.2024 Herzinfarkt Nachrichten

Bei Menschen mit Typ-2-Diabetes sind die Chancen, einen Myokardinfarkt zu überleben, in den letzten 15 Jahren deutlich gestiegen – nicht jedoch bei Betroffenen mit Typ 1.

15% bedauern gewählte Blasenkrebs-Therapie

29.05.2024 Urothelkarzinom Nachrichten

Ob Patienten und Patientinnen mit neu diagnostiziertem Blasenkrebs ein Jahr später Bedauern über die Therapieentscheidung empfinden, wird einer Studie aus England zufolge von der Radikalität und dem Erfolg des Eingriffs beeinflusst.

Costims – das nächste heiße Ding in der Krebstherapie?

28.05.2024 Onkologische Immuntherapie Nachrichten

„Kalte“ Tumoren werden heiß – CD28-kostimulatorische Antikörper sollen dies ermöglichen. Am besten könnten diese in Kombination mit BiTEs und Checkpointhemmern wirken. Erste klinische Studien laufen bereits.

Update Innere Medizin

Bestellen Sie unseren Fach-Newsletter und bleiben Sie gut informiert.