The immunological aspect of medical mycology has tended to lag behind similar aspects of other fields. It appears, however, that immunologic proc esses in the fungus-infected host are essentially similar to those which occur in bacterial, viral, and other diseases of infectious etiology. The procedures and techniques for measuring immunologic reactions are, therefore, similar to those which have been established for the infectious diseases in general. Possibly because of the somewhat more highly differentiated structure of the fungi, the preparation of antigens for immunologic studies requires certain modifications. Except for this difference no really specialized knowledge ap pears to be necessary in the performance of immunologic tests. As in other infectious diseases, immunologic data are of diagnostic and prognostic consequence only when interpreted in the light of the limitations of the commonly used tests. In some instances negative results, such as negative tests for cutaneous sensitivity, are of greater significance in exclud ing a particular diagnosis than are positive tests in establishing it, as exempli fied by the tu berculin test and, similarly, by the coccidioidin test for coccidi oidomycosis. Immunologic studies, however, constitute an important part of the clinical evaluation in respect to diagnosis, prognosis, and management of many of the systemic mycoses. The systemic mycoses are insidiously developing, chronic, and often fatal diseases. They tend to simulate tuberculosis. Consequently, there are many pathologic and immunologic analogies between the mycoses and chronic bacterial diseases. The pathogenic fungi may, on the one hand, be characterized as being more allergenic than bacteria, in the sense that cutaneous sensitivity is practically a constant feature of the human mycoses. On the other hand, they may be said to be less antigenic than many bacterial pathogens in that concentrations of circulating antibodies, expressed as antibody titers, are generally low. For example, although a positive complement-fixation test with undiluted serum or serum diluted 1 : 2 might be skeptically regarded in other infections, such low titers may assume diagnostic significance in the human mycoses, as is the case in blastomycosis ( 1 ) . The reasons for this mea ger antigenicity are not well known. It is possible that the slow progression