Literature DB >> 1651571

Evidence for arsenic as the immunosuppressive component of gallium arsenide.

L A Burns1, E E Sikorski, J J Saady, A E Munson.   

Abstract

Gallium arsenide (GaAs) has been shown previously to suppress the in vivo antibody-forming cell (AFC) response to sheep erythrocytes (SRBC) when administered intratracheally at concentrations between 50 and 200 mg/kg. In the present studies, direct addition of GaAs to in vitro-generated antibody cultures resulted in dose-dependent suppression of the primary antibody response, and was only seen when GaAs was added within 36 hr following immunization. Using atomic absorption spectrophotometry on tissue samples from mice exposed to 200 mg/kg GaAs, arsenic concentrations were found to peak in the spleen at 24 hr and decline, whereas gallium concentrations continue to rise through 14 days. Concentrations of each metal in the spleen at 24 hr are comparable to the concentrations achieved for each metal when GaAs is added at 25 microM to the in vitro model system. The 24 hr time point was chosen for comparison because all in vivo-in vitro studies were conducted using spleens from mice 24 hr after GaAs exposure. NaAsO2 and Ga(NO3)3 suppressed the AFC response dose-dependently, and in a time-dependent manner similar to GaAs when added to the in vitro system. However, based on IC50 values for each salt, the role of the gallium component in the immunosuppression appears weak. Oxalic acid (OA) and meso-2,3-dimercaptosuccinic acid (DMSA), chelators of gallium and arsenic respectively, were added to cultures with GaAs to confirm that arsenic was the primary immunosuppressive component. DMSA dose-dependently blocked GaAs-induced immunosuppression in vitro, while OA had no effect. The metal-binding compounds were determined to be specific for the metals used in these studies and did not cross-react with one another. DMSA was evaluated for its ability to prevent suppression of the AFC response in splenocytes from GaAs-exposed mice and was able to block GaAs-induced suppression of the AFC response when given sc every 4 hr beginning 1 hr prior to GaAs exposure. These data indicate that the arsenic component of GaAs is the major contributor to the GaAs-induced immunosuppression and that this effect occurs within the first 36 hr of the 5-day culture period in a concentration-dependent manner.

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Year:  1991        PMID: 1651571     DOI: 10.1016/0041-008x(91)90298-s

Source DB:  PubMed          Journal:  Toxicol Appl Pharmacol        ISSN: 0041-008X            Impact factor:   4.219


  7 in total

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Authors:  Zhifa Liu; Changhe Yuan; Stephen B Pruett
Journal:  Toxicol Sci       Date:  2012-06-13       Impact factor: 4.849

2.  Low-dose synergistic immunosuppression of T-dependent antibody responses by polycyclic aromatic hydrocarbons and arsenic in C57BL/6J murine spleen cells.

Authors:  Qian Li; Fredine T Lauer; Ke Jian Liu; Laurie G Hudson; Scott W Burchiel
Journal:  Toxicol Appl Pharmacol       Date:  2010-03-28       Impact factor: 4.219

Review 3.  Medical applications and toxicities of gallium compounds.

Authors:  Christopher R Chitambar
Journal:  Int J Environ Res Public Health       Date:  2010-05-10       Impact factor: 3.390

4.  Establishment of an immunoglobulin m antibody-forming cell response model for characterizing immunotoxicity in primary human B cells.

Authors:  Haitian Lu; Robert B Crawford; Colin M North; Barbara L F Kaplan; Norbert E Kaminski
Journal:  Toxicol Sci       Date:  2009-09-18       Impact factor: 4.849

5.  Arsenic exposure and human papillomavirus response in non-melanoma skin cancer Mexican patients: a pilot study.

Authors:  J Alberto Rosales-Castillo; Leonor C Acosta-Saavedra; Rosantina Torres; Jesús Ochoa-Fierro; Víctor H Borja-Aburto; Lizbeth Lopez-Carrillo; Gonzalo G Garcia-Vargas; Georgina B Gurrola; Mariano E Cebrian; Emma S Calderón-Aranda
Journal:  Int Arch Occup Environ Health       Date:  2004-07-03       Impact factor: 3.015

6.  Immunotoxicity and biodistribution analysis of arsenic trioxide in C57Bl/6 mice following a 2-week inhalation exposure.

Authors:  Scott W Burchiel; Leah A Mitchell; Fredine T Lauer; Xi Sun; Jacob D McDonald; Laurie G Hudson; Ke Jian Liu
Journal:  Toxicol Appl Pharmacol       Date:  2009-10-02       Impact factor: 4.219

7.  Early life arsenic exposure and acute and long-term responses to influenza A infection in mice.

Authors:  Kathryn A Ramsey; Rachel E Foong; Peter D Sly; Alexander N Larcombe; Graeme R Zosky
Journal:  Environ Health Perspect       Date:  2013-08-22       Impact factor: 9.031

  7 in total

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