Presence of IgE antibodies to bovine serum albumin in a patient developing anaphylaxis after vaccination with human peptide-pulsed dendritic cells

被引:200
作者
Mackensen, A
Dräger, R
Schlesier, M
Mertelsmann, R
Lindemann, A
机构
[1] Univ Freiburg, Med Ctr, Dept Hematol Oncol, D-79106 Freiburg, Germany
[2] Univ Freiburg, Med Ctr, Dept Rheumatol Clin Immunol, D-79106 Freiburg, Germany
关键词
dendritic cells; tumor immunotherapy; vaccination; anaphylactic reaction;
D O I
10.1007/s002620050614
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Dendritic cells are professional antigen-presenting cells that can be generated in vitro either from monocytes or from CD34(+) peripheral blood progenitor cells by using recombinant cytokines. These cells have potential implications for immunotherapeutic approaches in the treatment of cancer and other diseases. We have conducted a phase I study in melanoma patients using peptide-pulsed dendritic cells cultured in medium supplemented with 10% fetal calf serum (FCS) and a cocktail of cytokines. Peptide-pulsed dendritic cells were injected intravenously at 2-week intervals. Here we report on a case of type I hypersensitivity anaphylactic reaction after repetitive vaccination with autologous peptide-pulsed cells. Pre-vaccination and post-vaccination serum samples were evaluated for the presence of antibodies to FCS and bovine serum albumin (BSA). A rotrospective study in 7 patients vaccinated with FCS-cultured dendritic cells demonstrated the presence of IgG and IgM antibodies to FCS and BSA after vaccination in 6 out of 7 patients. However, IgE antibodies were absent in all patients with the exception of the patient developing anaphylaxis. The patient's serum was demonstrated to contain a strong IgE response directed against BSA. In contrast, 2 patients vaccinated with dendritic cells cultured under serum-free Conditions developed no antibodies to FCS and BSA after repetitive vaccination. We suggest that patients can be sensitized with an IgE response against BSA leading to anaphylactic reactions. On the basis of these data, dendritic cells cultured in autologous serum or under serum-free conditions are recommended for therapeutic applications in vivo.
引用
收藏
页码:152 / 156
页数:5
相关论文
共 21 条
  • [1] Dendritic cells and the control of immunity
    Banchereau, J
    Steinman, RM
    [J]. NATURE, 1998, 392 (6673) : 245 - 252
  • [2] COMPARISON BETWEEN RAST AND PHARMACIA CAP SYSTEM - A NEW AUTOMATED SPECIFIC IGE ASSAY
    BOUSQUET, J
    CHANEZ, P
    CHANAL, I
    MICHEL, FB
    [J]. JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 1990, 85 (06) : 1039 - 1043
  • [3] Rapid generation of broad T-cell immunity in humans after a single injection of mature dendritic cells
    Dhodapkar, MV
    Steinman, RM
    Sapp, M
    Desai, H
    Fossella, C
    Krasovsky, J
    Donahoe, SM
    Dunbar, PR
    Cerundolo, V
    Nixon, DF
    Bhardwaj, N
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1999, 104 (02) : 173 - 180
  • [4] SPECIFIC CYTOTOXIC LYMPHOCYTES AGAINST SYNGENEIC TUMORS ARE GENERATED IN CULTURE IN PRESENCE OF SYNGENEIC, BUT NOT XENOGENEIC, SERUM
    FOGEL, M
    SEGAL, S
    GORELIK, E
    FELDMAN, M
    [J]. INTERNATIONAL JOURNAL OF CANCER, 1978, 22 (03) : 329 - 334
  • [5] FORNI G, 1976, J IMMUNOL, V116, P1561
  • [6] Garbe A, 1998, BLOOD, V92, p165A
  • [7] In vitro differentiation of CD34(+) hematopoietic progenitor cells toward distinct dendritic cell subsets of the birbeck granule and MIIC-positive Langerhans cell and the interdigitating dendritic cell type
    Herbst, B
    Kohler, G
    Mackensen, A
    Veelken, H
    Kulmburg, P
    Rosenthal, FM
    Schaefer, HE
    Mertelsmann, R
    Fisch, P
    Lindemann, A
    [J]. BLOOD, 1996, 88 (07) : 2541 - 2548
  • [8] CD83+ blood dendritic cells as a vaccine for immunotherapy of metastatic renal-cell cancer
    Höltl, L
    Rieser, C
    Papesh, C
    Ramoner, R
    Bartsch, G
    Thurnher, M
    [J]. LANCET, 1998, 352 (9137) : 1358 - 1358
  • [9] Vaccination of patients with B-cell lymphoma using autologous antigen-pulsed dendritic cells
    Hsu, FJ
    Benike, C
    Fagnoni, F
    Liles, TM
    Czerwinski, D
    Taidi, B
    Engleman, EG
    Levy, R
    [J]. NATURE MEDICINE, 1996, 2 (01) : 52 - 58
  • [10] Hu XY, 1996, CANCER RES, V56, P2479