Literature DB >> 2191681

Lymphokine gene therapy for cancer.

S J Russell1.   

Abstract

The plethora of recombinant lymphokines that have recently become available has led to renewed hope for an immunotherapeutic solution to cancer. Many lymphokines, either singly or in combination, have already shown promise in animal trials and in preliminary human trials. Systemic lymphokine toxicity has been the major constraint on this type of therapy, often precluding the use of doses sufficient to induce tumour regression. To realize the therapeutic potential of recombinant lymphokines against cancer, alternative modes of delivery are needed which maximally stimulate local anti-tumour responses whilst causing minimal systemic toxicity. In this article, Stephen Russell proposes that tumour cell targeted lymphokine gene therapy would optimize lymphokine delivery. Some of the practical difficulties likely to be encountered with such an approach are also discussed.

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2191681     DOI: 10.1016/0167-5699(90)90081-j

Source DB:  PubMed          Journal:  Immunol Today        ISSN: 0167-5699


  13 in total

1.  Cloning and sequencing of defective particles derived from the autonomous parvovirus minute virus of mice for the construction of vectors with minimal cis-acting sequences.

Authors:  N Clément; B Avalosse; K El Bakkouri; T Velu; A Brandenburger
Journal:  J Virol       Date:  2001-02       Impact factor: 5.103

2.  Prevention of murine breast cancer by vaccination with tumor cells modified by cytokine-producing recombinant vaccinia viruses.

Authors:  G R Peplinski; K Tsung; J B Meko; J A Norton
Journal:  Ann Surg Oncol       Date:  1996-01       Impact factor: 5.344

3.  Retroviral vectors displaying functional antibody fragments.

Authors:  S J Russell; R E Hawkins; G Winter
Journal:  Nucleic Acids Res       Date:  1993-03-11       Impact factor: 16.971

4.  Use of an autonomous parvovirus vector for selective transfer of a foreign gene into transformed human cells of different tissue origins and its expression therein.

Authors:  F Dupont; L Tenenbaum; L P Guo; P Spegelaere; M Zeicher; J Rommelaere
Journal:  J Virol       Date:  1994-03       Impact factor: 5.103

5.  Transformation-dependent expression of interleukin genes delivered by a recombinant parvovirus.

Authors:  S J Russell; A Brandenburger; C L Flemming; M K Collins; J Rommelaere
Journal:  J Virol       Date:  1992-05       Impact factor: 5.103

6.  Chemo-immunotherapy of murine solid tumors: enhanced therapeutic effects by interleukin-2 combined with interferon alpha and the role of specific T cells.

Authors:  E Kedar; Y Rutkowski; B Leshem
Journal:  Cancer Immunol Immunother       Date:  1992       Impact factor: 6.968

7.  Induction of cellular immunity in chimpanzees to human tumor-associated antigen mucin by vaccination with MUC-1 cDNA-transfected Epstein-Barr virus-immortalized autologous B cells.

Authors:  G Pecher; O J Finn
Journal:  Proc Natl Acad Sci U S A       Date:  1996-02-20       Impact factor: 11.205

8.  Persistence of dormant tumor cells in the bone marrow of tumor cell-vaccinated mice correlates with long-term immunological protection.

Authors:  K Khazaie; S Prifti; P Beckhove; A Griesbach; S Russell; M Collins; V Schirrmacher
Journal:  Proc Natl Acad Sci U S A       Date:  1994-08-02       Impact factor: 11.205

9.  Construction and expression in tumor cells of a recombinant vaccinia virus encoding human interleukin-1 beta.

Authors:  G R Peplinski; K Tsung; E D Whitman; J B Meko; J A Norton
Journal:  Ann Surg Oncol       Date:  1995-03       Impact factor: 5.344

10.  Immunotherapy of malignancy by in vivo gene transfer into tumors.

Authors:  G E Plautz; Z Y Yang; B Y Wu; X Gao; L Huang; G J Nabel
Journal:  Proc Natl Acad Sci U S A       Date:  1993-05-15       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.