ToxSci Advance Access originally published online on October 5, 2005
Toxicological Sciences 2006 89(1):135-144; doi:10.1093/toxsci/kfj006
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Effects of Prenatal Exposure to Cigarette Smoke on Offspring Tumor Susceptibility and Associated Immune Mechanisms
* New York University School of Medicine, Nelson Institute of Environmental Medicine, Tuxedo, New York 10987; SUNY Upstate Medical University, Department of Microbiology & Immunology, Syracuse, New York 13210
Received August 11, 2005; accepted September 22, 2005
Epidemiologic evidence suggests that prenatal exposure to intact (unfractionated) cigarette smoke (CS) increases the incidence of cancer in the offspring. A toxicology study was carried out to examine the effects and underlying mechanisms of prenatal exposure to mainstream cigarette smoke (MCS) on offspring resistance to tumor challenge and surveillance mechanisms critical for the recognition and destruction of tumors. Pregnant B6C3F1 mice were exposed by inhalation to MCS for 5 days/week (4 h/day from gestational day 4 to parturition). Smoke-induced effects on offspring—host resistance to transplanted tumor cells; natural killer (NK) cell and cytotoxic T-lymphocyte (CTL) activity; cytokine levels; lymphoid organ immune cell subpopulations; and histology—were examined in 5-, 10- and 20-week-old male and female offspring. At a concentration of smoke roughly equivalent to smoking <1 pack of cigarettes/day, prenatally exposed male offspring challenged at 5 week of age with EL4 lymphoma cells demonstrated a greater than two-fold increase in tumor incidence (relative to age-/gender-matched air-exposed offspring); tumors in prenatally smoke-exposed pups also grew significantly faster. Cytotoxic T-lymphocyte activity in the smoke-exposed 5- and 10-week-old male pups was significantly less than that of the age- and gender-matched controls. No effects of prenatal CS exposure were observed on offspring NK activity, cytokine levels, lymphoid organ histology, or immune cell subpopulations. Results demonstrated that exposure of pregnant mice to a relevant dose of MCS decreased offspring resistance against transplanted tumor cells and persistently reduced CTL activity in prenatally exposed pups. This study provides biological plausibility for the epidemiologic data indicating that children of mothers who smoke during pregnancy have a greater risk of developing cancer in later life.
Key Words: cigarette smoke; developmental immunotoxicology; tumor surveillance mechanisms.
CiteULike 
Connotea 
Del.icio.us What's this?
This article has been cited by other articles:
|
|
 |
|
  M. K. Selgrade Immunotoxicity The Risk is Real Toxicol. Sci., December 1, 2007; 100(2): 328 - 332. [Abstract] [Full Text] [PDF]
|
|
|
|
 |
|
 S. P. Ng, B. G. Steinetz, S. G. Lasano, and J. T. Zelikoff Hormonal Changes Accompanying Cigarette Smoke-Induced Preterm Births in a Mouse Model Experimental Biology and Medicine, September 1, 2006; 231(8): 1403 - 1409. [Abstract] [Full Text] [PDF]
|
|