Methods for inducing sustained immune response
A method for promoting a sustained increased level of T-cell production in immunocompromised subjects in which method enkephalin peptides are administered according to an intermittent dose schedule. In particular, the method involves treatment of immunocompromised patients which includes the administration of enkephalin, either alone or in conjunction with other therapies, in an initial dosage regimen, with periodic booster dosages of enkephalin as necessary to maintain sustained immune system response.
1. A method of treatment of an immunocompromised patient, which method comprises:
(a) administering an enkephalin peptide comprising SEQ ID NO: 1, either alone or in conjunction with other therapies, in an initial dosage regimen, wherein each dose in the regimen is 1 to 250 μg/Kg bodyweight of the patient, said initial dosage regimen inducing an immune system response in the patient,
(b) discontinuing said initial dosage regimen with no further administration of said enkephalin peptide for a period of 4 to 24 weeks, wherein the immune system response is sustained during said period in which said administration of said enkephalin peptide is discontinued, and wherein said sustained immune system response comprises an elevated amount of at least one selected from the group consisting of cytotoxic T cells, natural killer cells, CD38 cells and interleukin II receptor expression in comparison to a baseline value,
(c) administering booster dosages of said enkephalin peptide thereafter as necessary to maintain the sustained immune system response.
2. The method of claim 1 , wherein the dosage of enkephalin peptide during the initial dosage regimen is 20 μg/Kg bodyweight of the patient.
3. The method of claim 1 , wherein the need for periodic booster shots is determined by measuring the patient's sustained immune response from 4 to 16 weeks after cessation of the initial dosage regimen, and comparing the sustained immune response with both the baseline value and a response value measured at the end of the dosing schedule.
4. The method of claim 1 , wherein periodic booster dosages are given, as needed, up to 5 times a week for 1 to 4 weeks.
5. The method of claim 1 , wherein the booster dosage of enkephalin peptide after the initial dosage regimen ranges from 20 to 100 μg/Kg bodyweight.
6. The method of claim 1 , wherein the initial dosage regimen is 1-5 times per week over a 4-12 week period.
7. The method of treatment of claim 1 , wherein the other therapies include cytokine, antiviral, antibiotics, antifungal, antiparasite and anti-tumor therapies.
8. The method of claim 1 , wherein said initial dosage regime is once per week for 4 to 12 weeks.