Abstract
The B cell repertoire was studied in intestinal mononuclear cells from normal individuals and patients with inflammatory bowel disease (IBD) by examining Ig heavy chain variable gene (V(H)) usage. Using reverse transcription of intestinal mucosal RNA followed by polymerase chain reaction with primers specific for each V(H) family and a housekeeping gene, a semiquantitative assay of V(H) family content in RNA samples was developed. While all V(H) family members were expressed, differences in V(H) usage in lamina propria intestinal B cells were noted between Crohn's disease, ulcerative colitis, and normal individuals. mRNA transcripts for V(H)4 were present at seemingly higher levels than their genomic representation and transcripts for V(H)4 and V(H)4 appeared to have higher levels in active, compared to inactive, IBD. Thus, within the massive polyclonal intestinal B cell response, there is a skewed V(H) usage which may be relevant to the antigenic and/or autoimmune response noted in IBD.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 240-245 |
| Number of pages | 6 |
| Journal | Clinical Immunology and Immunopathology |
| Volume | 71 |
| Issue number | 2 |
| DOIs | |
| State | Published - Jan 1 1994 |
| Externally published | Yes |
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ASJC Scopus subject areas
- Immunology and Allergy
- Pathology and Forensic Medicine
- Immunology
Cite this
Immunoglobulin variable region usage in human intestinal B lymphocytes. / McCabe, Robert P.; Carroll, William L.; Egan, Maureen; Cohn, Steven; Peters, Marion.
In: Clinical Immunology and Immunopathology, Vol. 71, No. 2, 01.01.1994, p. 240-245.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Immunoglobulin variable region usage in human intestinal B lymphocytes
AU - McCabe, Robert P.
AU - Carroll, William L.
AU - Egan, Maureen
AU - Cohn, Steven
AU - Peters, Marion
PY - 1994/1/1
Y1 - 1994/1/1
N2 - The B cell repertoire was studied in intestinal mononuclear cells from normal individuals and patients with inflammatory bowel disease (IBD) by examining Ig heavy chain variable gene (V(H)) usage. Using reverse transcription of intestinal mucosal RNA followed by polymerase chain reaction with primers specific for each V(H) family and a housekeeping gene, a semiquantitative assay of V(H) family content in RNA samples was developed. While all V(H) family members were expressed, differences in V(H) usage in lamina propria intestinal B cells were noted between Crohn's disease, ulcerative colitis, and normal individuals. mRNA transcripts for V(H)4 were present at seemingly higher levels than their genomic representation and transcripts for V(H)4 and V(H)4 appeared to have higher levels in active, compared to inactive, IBD. Thus, within the massive polyclonal intestinal B cell response, there is a skewed V(H) usage which may be relevant to the antigenic and/or autoimmune response noted in IBD.
AB - The B cell repertoire was studied in intestinal mononuclear cells from normal individuals and patients with inflammatory bowel disease (IBD) by examining Ig heavy chain variable gene (V(H)) usage. Using reverse transcription of intestinal mucosal RNA followed by polymerase chain reaction with primers specific for each V(H) family and a housekeeping gene, a semiquantitative assay of V(H) family content in RNA samples was developed. While all V(H) family members were expressed, differences in V(H) usage in lamina propria intestinal B cells were noted between Crohn's disease, ulcerative colitis, and normal individuals. mRNA transcripts for V(H)4 were present at seemingly higher levels than their genomic representation and transcripts for V(H)4 and V(H)4 appeared to have higher levels in active, compared to inactive, IBD. Thus, within the massive polyclonal intestinal B cell response, there is a skewed V(H) usage which may be relevant to the antigenic and/or autoimmune response noted in IBD.
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U2 - 10.1006/clin.1994.1078
DO - 10.1006/clin.1994.1078
M3 - Article
C2 - 7514115
AN - SCOPUS:0028353696
VL - 71
SP - 240
EP - 245
JO - Clinical Immunology
JF - Clinical Immunology
SN - 1521-6616
IS - 2
ER -