HLA Class II influences humoral autoimmunity in patients with type 2 autoimmune hepatitis
Type 2 autoimmune hepatitis (AIH) is characterized by the presence of anti-liver kidney microsome (anti-LKM-1) and/or anti-liver cytosol type 1 (anti-LC1) autoantibodies. However, the correlation between these autoantibodies and the genetic background has not been studied. Frequencies of HLA class I...
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Published in | Journal of hepatology Vol. 45; no. 6; pp. 844 - 850 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
Oxford
Elsevier B.V
01.12.2006
Elsevier |
Subjects | |
Online Access | Get full text |
ISSN | 0168-8278 1600-0641 |
DOI | 10.1016/j.jhep.2006.07.034 |
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Abstract | Type 2 autoimmune hepatitis (AIH) is characterized by the presence of anti-liver kidney microsome (anti-LKM-1) and/or anti-liver cytosol type 1 (anti-LC1) autoantibodies. However, the correlation between these autoantibodies and the genetic background has not been studied.
Frequencies of HLA class II alleles were compared between the 60 Caucasian children with type 2 AIH and 313 control subjects. The anti-LKM1 antibody reactivity directed against antigenic sites of CYP2D6 was analysed by ELISA.
HLA-DQB1∗0201 allele was found to be the primary genetic determinant of susceptibility to type 2 AIH by conferring the highest odd-ratio (OR
=
6.4). HLA-DRB1∗03 allele was significantly increased (
P
<
0.0001) among patients with both anti-LKM1 and anti-LC1 autoantibodies as well as in those with only anti-LC1
+ compared to those with anti-LKM1
+ alone. In contrast, HLA-DRB1∗07 allele was significantly associated (
P
<
0.0001) with anti-LKM1
+ alone compared to groups with both anti-LKM and anti-LC1 or with LC1+ alone. Children with the DRB1∗07 allele develop anti-LKM1 autoantibodies having a more restricted specificity (2 epitopes) than to those having HLA-DRB1∗03 allele (5 epitopes).
The HLA-DR locus is involved in autoantibody expression, while the DQ locus appears to be a critical determinant for the development of type 2 AIH. |
---|---|
AbstractList | Type 2 autoimmune hepatitis (AIH) is characterized by the presence of anti-liver kidney microsome (anti-LKM-1) and/or anti-liver cytosol type 1 (anti-LC1) autoantibodies. However, the correlation between these autoantibodies and the genetic background has not been studied.
Frequencies of HLA class II alleles were compared between the 60 Caucasian children with type 2 AIH and 313 control subjects. The anti-LKM1 antibody reactivity directed against antigenic sites of CYP2D6 was analysed by ELISA.
HLA-DQB1 *0201 allele was found to be the primary genetic determinant of susceptibility to type 2 AIH by conferring the highest odd-ratio (OR = 6.4). HLA-DRB1 *03 allele was significantly increased (P < 0.0001) among patients with both anti-LKM1 and anti-LC1 autoantibodies as well as in those with only anti-LC1(+) compared to those with anti-LKM1(+) alone. In contrast, HLA-DRB1 *07 allele was significantly associated (P < 0.0001) with anti-LKM1(+) alone compared to groups with both anti-LKM and anti-LC1 or with LC1+ alone. Children with the DRB1 *07 allele develop anti-LKM1 autoantibodies having a more restricted specificity (2 epitopes) than to those having HLA-DRB1 *03 allele (5 epitopes).
The HLA-DR locus is involved in autoantibody expression, while the DQ locus appears to be a critical determinant for the development of type 2 AIH. Type 2 autoimmune hepatitis (AIH) is characterized by the presence of anti-liver kidney microsome (anti-LKM-1) and/or anti-liver cytosol type 1 (anti-LC1) autoantibodies. However, the correlation between these autoantibodies and the genetic background has not been studied.BACKGROUND/AIMSType 2 autoimmune hepatitis (AIH) is characterized by the presence of anti-liver kidney microsome (anti-LKM-1) and/or anti-liver cytosol type 1 (anti-LC1) autoantibodies. However, the correlation between these autoantibodies and the genetic background has not been studied.Frequencies of HLA class II alleles were compared between the 60 Caucasian children with type 2 AIH and 313 control subjects. The anti-LKM1 antibody reactivity directed against antigenic sites of CYP2D6 was analysed by ELISA.METHODSFrequencies of HLA class II alleles were compared between the 60 Caucasian children with type 2 AIH and 313 control subjects. The anti-LKM1 antibody reactivity directed against antigenic sites of CYP2D6 was analysed by ELISA.HLA-DQB1 *0201 allele was found to be the primary genetic determinant of susceptibility to type 2 AIH by conferring the highest odd-ratio (OR = 6.4). HLA-DRB1 *03 allele was significantly increased (P < 0.0001) among patients with both anti-LKM1 and anti-LC1 autoantibodies as well as in those with only anti-LC1(+) compared to those with anti-LKM1(+) alone. In contrast, HLA-DRB1 *07 allele was significantly associated (P < 0.0001) with anti-LKM1(+) alone compared to groups with both anti-LKM and anti-LC1 or with LC1+ alone. Children with the DRB1 *07 allele develop anti-LKM1 autoantibodies having a more restricted specificity (2 epitopes) than to those having HLA-DRB1 *03 allele (5 epitopes).RESULTSHLA-DQB1 *0201 allele was found to be the primary genetic determinant of susceptibility to type 2 AIH by conferring the highest odd-ratio (OR = 6.4). HLA-DRB1 *03 allele was significantly increased (P < 0.0001) among patients with both anti-LKM1 and anti-LC1 autoantibodies as well as in those with only anti-LC1(+) compared to those with anti-LKM1(+) alone. In contrast, HLA-DRB1 *07 allele was significantly associated (P < 0.0001) with anti-LKM1(+) alone compared to groups with both anti-LKM and anti-LC1 or with LC1+ alone. Children with the DRB1 *07 allele develop anti-LKM1 autoantibodies having a more restricted specificity (2 epitopes) than to those having HLA-DRB1 *03 allele (5 epitopes).The HLA-DR locus is involved in autoantibody expression, while the DQ locus appears to be a critical determinant for the development of type 2 AIH.CONCLUSIONSThe HLA-DR locus is involved in autoantibody expression, while the DQ locus appears to be a critical determinant for the development of type 2 AIH. Type 2 autoimmune hepatitis (AIH) is characterized by the presence of anti-liver kidney microsome (anti-LKM-1) and/or anti-liver cytosol type 1 (anti-LC1) autoantibodies. However, the correlation between these autoantibodies and the genetic background has not been studied. Frequencies of HLA class II alleles were compared between the 60 Caucasian children with type 2 AIH and 313 control subjects. The anti-LKM1 antibody reactivity directed against antigenic sites of CYP2D6 was analysed by ELISA. HLA-DQB1∗0201 allele was found to be the primary genetic determinant of susceptibility to type 2 AIH by conferring the highest odd-ratio (OR = 6.4). HLA-DRB1∗03 allele was significantly increased ( P < 0.0001) among patients with both anti-LKM1 and anti-LC1 autoantibodies as well as in those with only anti-LC1 + compared to those with anti-LKM1 + alone. In contrast, HLA-DRB1∗07 allele was significantly associated ( P < 0.0001) with anti-LKM1 + alone compared to groups with both anti-LKM and anti-LC1 or with LC1+ alone. Children with the DRB1∗07 allele develop anti-LKM1 autoantibodies having a more restricted specificity (2 epitopes) than to those having HLA-DRB1∗03 allele (5 epitopes). The HLA-DR locus is involved in autoantibody expression, while the DQ locus appears to be a critical determinant for the development of type 2 AIH. |
Author | Debray, Dominique Fakhfakh, Amin Caillat-Zucman, Sophie Alvarez, Fernando Louafi, Hamida Djilali-Saiah, Idriss |
Author_xml | – sequence: 1 givenname: Idriss surname: Djilali-Saiah fullname: Djilali-Saiah, Idriss email: djilali-saiah.idriss@recherche-ste-justine.qc.ca organization: Gastroenterology Division, Hôpital Sainte-Justine, Montreal, Que., Canada – sequence: 2 givenname: Amin surname: Fakhfakh fullname: Fakhfakh, Amin organization: Gastroenterology Division, Hôpital Sainte-Justine, Montreal, Que., Canada – sequence: 3 givenname: Hamida surname: Louafi fullname: Louafi, Hamida organization: Gastroenterology Division, Hôpital Sainte-Justine, Montreal, Que., Canada – sequence: 4 givenname: Sophie surname: Caillat-Zucman fullname: Caillat-Zucman, Sophie organization: INSERM U 561, Hôpital St-Vincent de Paul, Paris, France – sequence: 5 givenname: Dominique surname: Debray fullname: Debray, Dominique organization: Hepatology Unit, Hôpital Kremlin Bicêtre, Paris, France – sequence: 6 givenname: Fernando surname: Alvarez fullname: Alvarez, Fernando organization: Gastroenterology Division, Hôpital Sainte-Justine, Montreal, Que., Canada |
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Keywords | AIH LKM-1 Human Autoimmunity Antigens/Peptides/Epitopes SSP Autoantibodies ANA SMA MHC LC1 Immunopathology Antigenic determinant Peptides Major histocompatibility system Class II histocompatibility antigen Autoantibody Hepatic disease Autoimmune disease Hepatitis Digestive diseases Humoral immunity |
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SubjectTerms | Adolescent Alleles Antigens/Peptides/Epitopes Autoantibodies Autoantibodies - immunology Autoantigens - immunology Autoimmunity Biological and medical sciences Child Child, Preschool Cytochrome P-450 CYP2D6 - genetics Cytochrome P-450 CYP2D6 - immunology Cytochrome P-450 CYP2D6 - metabolism Epitopes Female Gastroenterology. Liver. Pancreas. Abdomen Genes, MHC Class II - genetics Genes, MHC Class II - immunology Genetic Predisposition to Disease Genotype Hepatitis, Autoimmune - genetics Hepatitis, Autoimmune - immunology Hepatitis, Autoimmune - metabolism HLA-DQ Antigens - genetics HLA-DQ beta-Chains HLA-DR Antigens - genetics HLA-DRB1 Chains Human Humans Infant Liver. Biliary tract. Portal circulation. Exocrine pancreas Male Medical sciences MHC Other diseases. Semiology |
Title | HLA Class II influences humoral autoimmunity in patients with type 2 autoimmune hepatitis |
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