Abstract
Four monoclonal antibodies (mAbs), UC-A4, UC-D3, UC-H9, and IL-A21, specific for bovine major histocompatibility complex class II proteins are described. Sequential immunoprecipitation experiments using biotin-labeled peripheral blood mononuclear cells suggested, but did not conclusively establish, that each of these antibodies recognized a different epitope. The epitope identified by IL-A21 appeared to be common to all of the class II proteins precipitated by the four mAbs, and UC-D3 and UC-H9 each appeared to react with distinct epitopes on separate subsets of these class II proteins. Monoclonal antibody UC-A4 appeared to identify an epitope on a subset of the class II molecules identified by UC-H9. Differences found in the expression by lymphoid cells of class II proteins identified by the four mAbs were indicative of each mAb recognizing a different epitope. UC-H9 and IL-A21 class II proteins were detected on all surface immunoglobulin (S'Ig) positive cells in peripheral blood, but UC-A4 and UC-D3 class II proteins were not. Expression of UC-A4 class II proteins, detected at low density on a strikingly reduced number of S'Ig+ cells from the blood of some bovine leukosis virus-infected cattle, could be increased by culturing these B cells with lipopolysaccharide. All peripheral blood monocytes expressed UC-H9 and IL-A21 class II proteins, but only a proportion of monocytes expressed detectable UC-A4 and UC-D3 class II proteins. Almost all mitogen-stimulated BoCD4+ and BoCD8+ T cells expressed UC-H9 and IL-A21 class II proteins, whereas fewer stimulated T cells of both subsets expressed UC-A4 and UC-D3 class II proteins. All gamma/delta receptor (γ/δ R) T cells expressed UC- D3, UC-H9, and IL-A21 class II proteins, but no cells (of γ/δ R+ or CD4+/CD2+ phenotype) from γ/δ R+ T cell-enriched cultures expressed UC- A4 class II proteins.
| Original language | English (US) |
|---|---|
| Pages (from-to) | 479-489 |
| Number of pages | 11 |
| Journal | Journal of Leukocyte Biology |
| Volume | 53 |
| Issue number | 5 |
| State | Published - 1993 |
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Keywords
- B cells
- BoLA D
- monoclonal antibodies
- monocytes
- T cells
ASJC Scopus subject areas
- Cell Biology
Cite this
Differential expression of bovine MHC class II antigens identified by monoclonal antibodies. / Taylor, B. C.; Choi, K. Y.; Scibienski, R. J.; Moore, Peter F; Stott, Jeffrey L.
In: Journal of Leukocyte Biology, Vol. 53, No. 5, 1993, p. 479-489.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Differential expression of bovine MHC class II antigens identified by monoclonal antibodies
AU - Taylor, B. C.
AU - Choi, K. Y.
AU - Scibienski, R. J.
AU - Moore, Peter F
AU - Stott, Jeffrey L
PY - 1993
Y1 - 1993
N2 - Four monoclonal antibodies (mAbs), UC-A4, UC-D3, UC-H9, and IL-A21, specific for bovine major histocompatibility complex class II proteins are described. Sequential immunoprecipitation experiments using biotin-labeled peripheral blood mononuclear cells suggested, but did not conclusively establish, that each of these antibodies recognized a different epitope. The epitope identified by IL-A21 appeared to be common to all of the class II proteins precipitated by the four mAbs, and UC-D3 and UC-H9 each appeared to react with distinct epitopes on separate subsets of these class II proteins. Monoclonal antibody UC-A4 appeared to identify an epitope on a subset of the class II molecules identified by UC-H9. Differences found in the expression by lymphoid cells of class II proteins identified by the four mAbs were indicative of each mAb recognizing a different epitope. UC-H9 and IL-A21 class II proteins were detected on all surface immunoglobulin (S'Ig) positive cells in peripheral blood, but UC-A4 and UC-D3 class II proteins were not. Expression of UC-A4 class II proteins, detected at low density on a strikingly reduced number of S'Ig+ cells from the blood of some bovine leukosis virus-infected cattle, could be increased by culturing these B cells with lipopolysaccharide. All peripheral blood monocytes expressed UC-H9 and IL-A21 class II proteins, but only a proportion of monocytes expressed detectable UC-A4 and UC-D3 class II proteins. Almost all mitogen-stimulated BoCD4+ and BoCD8+ T cells expressed UC-H9 and IL-A21 class II proteins, whereas fewer stimulated T cells of both subsets expressed UC-A4 and UC-D3 class II proteins. All gamma/delta receptor (γ/δ R) T cells expressed UC- D3, UC-H9, and IL-A21 class II proteins, but no cells (of γ/δ R+ or CD4+/CD2+ phenotype) from γ/δ R+ T cell-enriched cultures expressed UC- A4 class II proteins.
AB - Four monoclonal antibodies (mAbs), UC-A4, UC-D3, UC-H9, and IL-A21, specific for bovine major histocompatibility complex class II proteins are described. Sequential immunoprecipitation experiments using biotin-labeled peripheral blood mononuclear cells suggested, but did not conclusively establish, that each of these antibodies recognized a different epitope. The epitope identified by IL-A21 appeared to be common to all of the class II proteins precipitated by the four mAbs, and UC-D3 and UC-H9 each appeared to react with distinct epitopes on separate subsets of these class II proteins. Monoclonal antibody UC-A4 appeared to identify an epitope on a subset of the class II molecules identified by UC-H9. Differences found in the expression by lymphoid cells of class II proteins identified by the four mAbs were indicative of each mAb recognizing a different epitope. UC-H9 and IL-A21 class II proteins were detected on all surface immunoglobulin (S'Ig) positive cells in peripheral blood, but UC-A4 and UC-D3 class II proteins were not. Expression of UC-A4 class II proteins, detected at low density on a strikingly reduced number of S'Ig+ cells from the blood of some bovine leukosis virus-infected cattle, could be increased by culturing these B cells with lipopolysaccharide. All peripheral blood monocytes expressed UC-H9 and IL-A21 class II proteins, but only a proportion of monocytes expressed detectable UC-A4 and UC-D3 class II proteins. Almost all mitogen-stimulated BoCD4+ and BoCD8+ T cells expressed UC-H9 and IL-A21 class II proteins, whereas fewer stimulated T cells of both subsets expressed UC-A4 and UC-D3 class II proteins. All gamma/delta receptor (γ/δ R) T cells expressed UC- D3, UC-H9, and IL-A21 class II proteins, but no cells (of γ/δ R+ or CD4+/CD2+ phenotype) from γ/δ R+ T cell-enriched cultures expressed UC- A4 class II proteins.
KW - B cells
KW - BoLA D
KW - monoclonal antibodies
KW - monocytes
KW - T cells
UR - http://www.scopus.com/inward/record.url?scp=0027256666&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=0027256666&partnerID=8YFLogxK
M3 - Article
C2 - 7684762
AN - SCOPUS:0027256666
VL - 53
SP - 479
EP - 489
JO - Journal of Leukocyte Biology
JF - Journal of Leukocyte Biology
SN - 0741-5400
IS - 5
ER -