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Effect of transfer factor on lymphocyte function in anergic patients
The Journal of Clinical Investigation
|November 1, 1972
Summary
Dialyzable transfer factor (DTF) can restore cell-mediated immunity in anergic patients. DTF induced delayed skin reactivity and macrophage migration inhibition factor (MIF) production, but not blastogenesis, suggesting specific immune cell activation.
Area of Science:
- Immunology
- Cellular Biology
Background:
- Chronic mucocutaneous candidiasis is characterized by anergy.
- Dialyzable transfer factor (DTF) is derived from leukocytes and may restore cell-mediated immunity.
Purpose of the Study:
- To evaluate the efficacy of DTF in anergic patients with chronic mucocutaneous candidiasis.
- To investigate the immunological responses following DTF administration.
Main Methods:
- Five anergic patients received DTF from a single donor.
- Immunological assessments included delayed cutaneous hypersensitivity, in vitro antigen-induced thymidine incorporation, and macrophage migration inhibition factor (MIF) production.
- Patients were tested before and after DTF injection.
Main Results:
- Four out of five patients developed delayed skin responses to antigens the donor was sensitive to.
- Recipient lymphocytes produced MIF upon exposure to specific antigens.
- Antigen-induced lymphocyte transformation was observed only intermittently in one patient.
- Attempts to sensitize patients with chlorodinitrobenzene were unsuccessful.
- A patient with Nezelof syndrome did not respond to DTF.
Conclusions:
- DTF enhances immunocompetent cells involved in lymphokine production.
- DTF has minimal effect on cells mediating blastogenesis.
- The specific immune effects of DTF were demonstrated by the failure to induce sensitization to chlorodinitrobenzene.
- The lack of response in Nezelof syndrome suggests lymphokine-producing cells are thymus-derived.