Publication | Open Access
Subsets of null and gamma delta T-cell receptor+ T lymphocytes in the blood of young pigs identified by specific monoclonal antibodies.
105
Citations
31
References
1992
Year
Laboratory ImmunologyLymphocyte DevelopmentImmunologyImmunodominanceImmunologic MechanismAntigen ProcessingNull Cell PopulationImmune SystemImmunotherapyRat Monoclonal AntibodiesLymphocyte BiologyAllergyAutoimmune DiseaseYoung PigsAutoimmunityT Cell ImmunityCell BiologyNull T CellsMedicineSpecific Monoclonal Antibodies
Rat monoclonal antibodies (mAb) against isolated pig Null T cells were derived using a novel two-colour cytofluorometric assay. One (MAC320) identified all blood CD2-sIg- 'Null' cells (present at up to approximately 6 x 10(6)/ml). Another type (MAC319 and MAC318) identified a subset comprising approximately 60% or approximately 30% of the Null cell population. This percentage appears genetically determined. This subset partially overlapped with a gamma delta T-cell receptor+ (TcR+) population which consisted of approximately 40% of Null T cells. The antibodies did not react with other leucocyte or lymphocyte populations. In non-reducing conditions, MAC320 precipitated two molecules at approximately 270,000-280,000 MW in SDS-PAGE; the larger of which was also precipitated by MAC319 (and MAC318, which binds to the same epitope). Under reducing conditions, MAC320 immunoprecipitated two or three polypeptide chains at approximately 130,000-160,000 MW; MAC319 precipitated only the largest of these polypeptides. The large MAC319+ MAC320+ molecule on one subset is removed by bromelain treatment; the smaller MAC319- MAC320+ molecule on the remaining Null cells is not bromelain sensitive. Several properties of this new antigen complex specific to pig Null T cells show that it is distinct from the ruminant T19 complex.
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A trans-acting major histocompatibility complex-linked gene whose alleles determine gain and loss changes in the antigenic structure of a classical class I molecule. Alexandra M. Livingstone, Simon J. Powis, Austin G. Diamond, The Journal of Experimental Medicine HistocompatibilityClassical ClassRat MhcGeneticsHla Immunogenetics | 1989 | 93 |
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