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K Vickerman

Publications and source records attributed to K Vickerman.

57 records · Page 4Linked to original sources

All metacyclic variable antigen types of Trypanosoma congolense identified using monoclonal antibodies.

Vaccination against the tsetse-borne trypanosomiases has proved impossible because of the trypanosome's ability to generate a seemingly inexhaustible number of variable antigen types in the blood or tissues of the host. Each variable antigen is a glycoprotein which forms a surface coat on the trypanosome and each glycoprotein is the product of a single gene. The full repertoire of such antigens has not been identified for any trypanosome serodeme (genotype) as yet, but the number of genes coding for variable antigen glycoproteins is estimated to be between 100 and 1,000. We have previously postulated that for Trypanosoma brucei the antigen repertoire of the infective metacyclic stage trypanosomes inoculated by the tsetse fly may be considerably smaller than that expressed in the mammalian host. If this is so then protection against infection by the vector becomes an easier proposition, but the actual scale of the metacyclic repertoire is also unknown. We present here evidence that the metacyclic repertoire of a stock of T. congolense, the most important of the pathogenic cattle trypanosomes, is limited to 12 variable antigen types.

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Instability of the Trypanosoma brucei rhodesiense metacyclic variable antigen repertoire.

Trypanosoma brucei rhodesiense undergoes antigenic variation in its mammalian host by changing the glycoprotein composing its surface coat. Trypanosome clones which have the same repertoire of variable antigen types (VATs) are said to belong to the same serodeme. Tsetse flies infected with a particular serodeme extrude infective metacyclic trypanosomes which express only a restricted part of this repertoire. As the only known acquired immunity in African trypanosomiasis is VAT-specific this limitation of metacyclic VAT (M-VAT) repertoire could be important in devising a vaccine. This possibility of immunoprophylaxis could depend, however, on whether or not the M-VAT repertoire is conserved over long periods of repeated cyclical transmission and between epidemics. Studies reported here on isolates made from an East African focus of sleeping sickness over a 20-yr period suggest substantial changes in the M-VATs expressed during this time. Furthermore, we have detected change in expression of 3 M-VATs during sequential tsetse transmission of a clone in the laboratory indicating a possible instability in the organization of M-VAT genes.

Animals↗