Transplant immunosuppression enhances efficiency of adenoviral-mediated gene retransfection: inhibition of interferon-gamma and immunoglobin G

Ann Thorac Surg. 2002 Apr;73(4):1092-7. doi: 10.1016/s0003-4975(01)03574-3.

Abstract

Background: Transplant immunosuppression regimen facilitates successful adenovirus-mediated gene transfection and retransfection in the rat lung. Herein, we investigated the effect of this strategy on circulating cytokines and antiadenoviral immunoglobin G antibody.

Methods: Male Lewis rats were transfected with 1 x 10(9) pfu/mL of E1-deleted Ad5CMVLacZ vector transtracheally. Rats were randomly assigned to receive daily intraperitoneal triple immunosuppression regimen consisting of cyclosporine (15 mg/kg per day), azathioprine (6 mg/kg per day), and methylprednisolone (2.5 mg/kg per day), or normal saline solution. Retransfection was performed 35 days later to all nonimmunosuppressed animals, whereas immunosuppressed rats were further randomized to receive retransfection or phosphate-buffered saline. Animals were sacrificed on days 1, 2, 7, 35, 42, and 49 after the initial transfection. Beta-galactosidase activity was measured on lung homogenates. Interferon-gamma, tumor necrosis factor-alpha, and antiadenoviral immunoglobin G were measured from the serum.

Results: Enhanced and prolonged transgene expression was observed in immunosuppressed animals, especially after retransfection. Concentrations of serum tumor necrosis factor-alpha in both groups were less than 12 pg/mL throughout the study. A significant increase in serum interferon-gamma levels was observed in nonimmunosuppressed animals after retransfection; this was not seen in the immunosuppressed animals. Serum antiadenoviral immunoglobin G titers in both groups were sharply elevated on day 1, and declined to basal levels by day 7, reflecting a preexisting level of humoral immunity to adenovirus. The titer in nonimmunosuppressed rats was significantly increased after retransfection, but remained at very low level in immunosuppressed animals.

Conclusions: Inhibition of interferon-gamma and antiadenoviral immunoglobin G production by triple immunosuppressants may be part of the mechanisms that lead to enhanced and prolonged transgene expression after retransfection.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenoviridae* / immunology
  • Animals
  • Antibodies, Viral / blood*
  • Azathioprine / pharmacology
  • Cyclosporine / pharmacology
  • Drug Therapy, Combination
  • Gene Expression / drug effects
  • Genetic Vectors*
  • Immunoglobulin G / blood*
  • Immunosuppression Therapy
  • Immunosuppressive Agents / administration & dosage*
  • Immunosuppressive Agents / pharmacology
  • Interferon-gamma / blood*
  • Lac Operon
  • Male
  • Methylprednisolone / pharmacology
  • Rats
  • Rats, Inbred Lew
  • Retreatment
  • Transfection*
  • Transgenes
  • Tumor Necrosis Factor-alpha / metabolism
  • beta-Galactosidase / genetics
  • beta-Galactosidase / metabolism

Substances

  • Antibodies, Viral
  • Immunoglobulin G
  • Immunosuppressive Agents
  • Tumor Necrosis Factor-alpha
  • Interferon-gamma
  • Cyclosporine
  • beta-Galactosidase
  • Azathioprine
  • Methylprednisolone