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RAISING ANTIBODIES T O PPD-COUPLED PEPTIDES 29 TABLE 1 Retention of '251-labelledPAS-PPDin the skin of BCG-positiveand BCG-negative guineaPigs Radioactivity recovered ( c . p . m . 4%) '2SI-labelled PAS-PPD (approx. ) was injected subcutaneously into each site of BCG-positive or BCG-negative guinea-pigs. In conjunction with Dr T . D. Kellaway, we raised antisera by injecting PPD in complete Freund's adjuvant into BCG-positive rabbits that reacted by immunoprecipitation with high concentrations of PPD.

Lachmann: That may well be so. McConnell: Another reason why PPD may act as such a good ccarrier is that perhaps there are no ‘suppressor’ determinants on PPD which are recognized by T suppressor cells. There is evidence for this for lysozyme. Suppressor cells and antibody recognize determinants in the same region of the molecule. Since 46 DISCUSSION PPD is not recognized by antibody, perhaps there isn’t a suppressor determinant on it. Lachmann: This is what we suggest from our T cell cloning data, but there is a substantial and confusing literature on suppressor T cells generated in response to tubercle bacilli.

J. ) LACHMANN ET AL 34 Immunization with PPD conjugates of peptides The putative leucotactic nonapeptide of the C3 a chain Analysis of the proteolytic fragmentation of the complement component C3 in different laboratories has shown that two closely related fragments of the a chain differ in the ability to induce leucocytosis in rabbits. Thus the C3d-k fragment (Meuth et a1 1983) is active whereas the physiological C3d,g fragment (Davis et a1 1984) is not. Sequence studies showed that these fragments differ in that C3d-k has an extra nine amino acids.

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