ABSTRACT
Twenty-one of the forty-two patients with osteomyelitis developing after a combined maxillofacial and craniocerebral injury were administered thymogen, an immunocorrective drug, as a component of combined therapy; immunologic indications for the prescription of such an agent were present in all these patients. Depressed T-cellular immunity was the principal disorder of the immunologic reactivity of this patient population; they also developed elevated counts of NK cells and increased interleukin synthesis by the macrophages, this reflecting a high activity of inflammation. Thymogen therapy was conducive to normalization of the immunologic and nonspecific reactivity and enhanced the treatment efficacy on the whole.
Subject(s)
Adjuvants, Immunologic/therapeutic use , Brain Injuries/therapy , Dipeptides , Maxillofacial Injuries/therapy , Multiple Trauma/therapy , Osteomyelitis/therapy , Brain Injuries/complications , Brain Injuries/immunology , Combined Modality Therapy , Drug Evaluation , Humans , Immunity, Cellular/drug effects , Immunity, Cellular/immunology , Maxillofacial Injuries/complications , Maxillofacial Injuries/immunology , Multiple Trauma/complications , Multiple Trauma/immunology , Osteomyelitis/etiology , Osteomyelitis/immunology , Peptides/therapeutic useABSTRACT
Forty-three patients with traumatic osteomyelitis developing after combined maxillofacial and craniocerebral injuries and thirty normal subjects were examined. Immunologic findings permit distinguishing two groups of patients: those with marked disorders of the T cellular immunity (reduced T helper and Tx counts, interleukin-2 synthesis, and Tx/T suppressor coefficient) and without such shifts. The therapy of patients without manifest immunity shifts was generally effective whereas in those with marked immunity disorders the therapy efficacy was inadequate and the immunity disorders persisted.