The timing of immunization affects the development of diabetes in rodents

被引:41
作者
Classen, JB
机构
[1] Classen Immunotherapies, Inc.
[2] Classen Immunotherapies, Inc., Baltimore, MD 21212
关键词
diabetes mellitus; insulin-dependent; mice; inbred NOD; rats; inbred BB; vaccination; vaccines; inactivated;
D O I
10.3109/08916939608995359
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Insulin-dependant diabetes mellitus (IDDM) is an autoimmune disease that can be altered by immune modulation, NOD mice and BE rats have been used as models of spontaneous IDDM. The development of diabetes in these animals has been altered by several different immune modulators using relatively high doses for the size of the animal. The effect of pharmaceutical doses of vaccines on the development of diabetes in these rodents has not been adequately studied. Methods: I studied the effect of administering killed human vaccines using low concentrations and as few as 3 doses. Results: Administration of human vaccines to diabetic prone newborn animals starting before 2 weeks of age prevented the development of diabetes while administration of the pertussis vaccine starting at 8 weeks of life was associated with an increased incidence of diabetes. Conclusions: Animal studies have demonstrated the timing and content of human vaccines can affect the development of diabetes. Clinical trials of new human vaccines are not designed and generally not powered to detect an effect of immunization on the development of IDDM, These animal toxicology studies indicate that the effect of vaccines on human insulin dependent diabetes needs to be examined,
引用
收藏
页码:137 / 145
页数:9
相关论文
共 22 条
  • [1] BURNSTEIN D, 1989, DIABETES, V38, P24
  • [2] CYCLOPHOSPHAMIDE-INDUCED DIABETES IN NOD WEHI MICE - EVIDENCE FOR SUPPRESSION IN SPONTANEOUS AUTOIMMUNE DIABETES-MELLITUS
    CHARLTON, B
    BACELJ, A
    SLATTERY, RM
    MANDEL, TE
    [J]. DIABETES, 1989, 38 (04) : 441 - 447
  • [3] POST-THYMECTOMY ORGAN-SPECIFIC AUTOIMMUNITY - ENHANCEMENT BY CYCLOSPORINE-A AND INHIBITION BY IL-2
    CLASSEN, JB
    SHEVACH, EM
    [J]. AUTOIMMUNITY, 1993, 15 (01) : 55 - 59
  • [4] AUTOIMMUNE DIABETES-MELLITUS IN THE BB RAT
    CRISA, L
    MORDES, JP
    ROSSINI, AA
    [J]. DIABETES-METABOLISM REVIEWS, 1992, 8 (01): : 9 - 37
  • [5] Foulis AK, 1996, DIABETOLOGIA, V39, P127
  • [6] ANDROGEN TREATMENT PREVENTS DIABETES IN NONOBESE DIABETIC MICE
    FOX, HS
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1992, 175 (05) : 1409 - 1412
  • [7] BETA-CELL EXPRESSION OF ENDOGENOUS XENOTROPIC RETROVIRUS DISTINGUISHES DIABETES-SUSCEPTIBLE NOD/LT FROM RESISTANT NON/LT MICE
    GASKINS, HR
    PROCHAZKA, M
    HAMAGUCHI, K
    SERREZE, DV
    LEITER, EH
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (06) : 2220 - 2227
  • [8] DEPLETION OF RT6.1+ LYMPHOCYTES-T INDUCES DIABETES IN RESISTANT BIOBREEDING WORCESTER (BB/W) RATS
    GREINER, DL
    MORDES, JP
    HANDLER, ES
    ANGELILLO, M
    NAKAMURA, N
    ROSSINI, AA
    [J]. JOURNAL OF EXPERIMENTAL MEDICINE, 1987, 166 (02) : 461 - 475
  • [9] ISLET EXPRESSION OF INTERFERON-ALPHA PRECEDES DIABETES IN BOTH THE BB RAT AND STREPTOZOTOCIN-TREATED MICE
    HUANG, XJ
    HULTGREN, B
    DYBDAL, N
    STEWART, TA
    [J]. IMMUNITY, 1994, 1 (06) : 469 - 478
  • [10] JAWORSKI MA, 1985, DIABETES S1, V34, pA72