Abstract
Humoral antibody, as an effector of homograft rejection, is most potent against dissociated tumor cell homografts. It is suggested that this unique vulnerability is a function of the dissociated state and rapid growth rate inherent in that type of homograft. On the other hand, delayed sensitivity and cell-bound immune factors appear to play a predominant role in the rejection of solid homografts. A mutually exclusive selection of delayed sensitivity over humoral antibody, or vice versa, is not warranted by the facts currently available, nor would such a selection serve any useful purpose. Humoral antibody may play a role in the rejection of orthotopic skin grafts, despite the difficulties encountered to date in its detection. From the evidence reviewed, however, it would appear that the role would be a subsidiary one.