Claims
- 1. A method of treating renal cell carcinoma comprising administering to a patient having same an effective, renal cell carcinoma-inhibiting amount of the immunoreactive, sensitized cells and administering to the patient an amount of cimetidine effective to inhibit the patient's suppresor cells
- wherein said immunoreactive, sensitized cells are prepared by a process comprising the steps of:
- (a) collecting mononuclear cells from the blood of an individual patient afflicted with renal cell carcinoma;
- (b) incubating the mononuclear cells with an effective amount of an H2 receptor antagonist and removing or chemically inactivating the suppressor T-cells from the mononuclear cells;
- (c) suspending the mononuclear cells of step (b) in culture medium and admixing the suspended mononuclear cells with autologous blood serum, a non-specific lymphocyte activator and an effective amount of an extract of the patient's tumor containing antigen specific to renal cell carcinoma;
- (d) culturing the admixture of step (c) under hyperthermic conditions of about 38.degree. C. to about 41.degree. C. in the presence of an amount of cimetidine effective to reduce suppressor cell activity for a period of time sufficient to activate and sensitize the mononuclear cells in vitro against the patient's renal cell carcinoma; and
- (e) irradiating the immunoreactive, sensitized cells with an effective amount of gamma radiation to re-deplete any radiosensitive suppressor cells that may be present in the culture of activated and immunized mononuclear cells, thereby providing immunoreactive, sensitized cells specific to the patient's renal cell carcinoma.
- 2. The method of claim 1 in which in step (c) the non-specific lymphocyte activator is phytohemagglutinin, interleukin 1, pokeweed mitogen, supernatants of human cells stimulated with phytohemagglutinin or pokeweed mitogen, a supernatant of a mixed lymphocyte culture, or a mixture of two or more of these activators.
- 3. The method of claim 2 in which the activator is a combination of phytohemagglutinin, a conditioned supernatant of a mixed lymphocyte culture and interleukin 2.
- 4. The method of claim 2 in which the activator is the conditioned supernatant of a mixed lymphocyte culture.
- 5. The method of claim 1 in which up to 2.4 grams/day of cimetidine is administered.
CROSS REFERENCE TO RELATED APPLICATIONS
This is a continuation of application Ser. No. 07/681,668, filed Apr. 8, 1991, which is a continuation of application Ser. No. 07/405,044, filed Sep. 11, 1989, which is a continuation of application Ser. No. 06/903,489, filed Sep. 4, 1986, which is a continuation-in-part of application Ser. No. 06/595,081, filed Mar. 30, 1984, all now abandoned.
US Referenced Citations (4)
Foreign Referenced Citations (1)
Number |
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8700054 |
Apr 1987 |
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Non-Patent Literature Citations (12)
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Continuations (3)
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681668 |
Apr 1991 |
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405044 |
Sep 1989 |
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903489 |
Sep 1986 |
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Continuation in Parts (1)
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595081 |
Mar 1984 |
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