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PubMed1984

Risk estimates of liver cancer due to aflatoxin exposure from peanuts and peanut products.

An assessment was undertaken of the risk of liver cancer in the USA associated with aflatoxin ingestion from peanuts. Both laboratory-animal data and epidemiological data collected from the scientific literature and several prominent mathematical extrapolation techniques were used. Risk estimates differed by a factor of greater than 1000 when the extrapolated results of three selected animal studies were analysed. Dose-response data for the male Fischer rat, the most sensitive mammalian species studied, produced an estimate of 158 cases of liver cancer per year in the USA at current levels of aflatoxin exposure. An estimate of 58 annual cases was predicted on the basis of epidemiological data of populations in Africa and Thailand.

Africa↗
PubMed1980

Peanut agglutinin. VI. Identification of murine T lymphocyte subsets during ontogenesis by use of peanut agglutinin and Ly-6.2 antiserum.

Fluoresceinated peanut agglutinin (PNA-FTC), Thy-1.2, and Ly-6.2 antisera were used to identify various murine T lymphocyte subpopulations during fetal and perinatal life. By means of double immunofluorescence labeling, we identified three T lymphocyte subsets: PNA+Ly-6.2+, PNA+Ly-6.2-, PNA-Ly-6.2+ having distinct distribution in the adult thymus and spleen. The study of the appearance of these three subsets in fetal liver, thymus, and spleen has shown that they did not occur similarly. The PNA+Ly-6.2+ subset was present in all three organs during fetal life and at a level rather similar to that of adult life; the PNA+Ly-6.2- subset was also present in the three fetal organs; conversely, the percentage of the PNA-Ly-6.2+ spleen cells was very low in fetal and neonatal life and increased significantly between 1 and 2 wk of age. Our results demonstrate that during fetal life, lymphocyte subsets are phenotypically differentiated as in adult life and that differentiation of T lymphocytes occurs preferentially through various lineages present during early ontogenesis. Moreover, quantitative modulation of some of these subsets is shown from fetal to adult life and may explain some of the immunologic immature features of young murine spleen.

Adrenal Cortex Hormones↗
PubMed1980

Peanut agglutinin. V. Thymocyte subpopulations in the mouse studied with peanut agglutinin and Ly-6.2 antiserum.

Thymocyte heterogeneity has been studied by the use of two cell surface markers--the Ly-6.2 alloantigen and peanut agglutinin (PNA) receptor. The previously described distribution of Ly-6 on corticoresistant and PNA binding to corticosensitive thymocytes has been confirmed. Double immunofluorescence labeling experiments in combination with techniques of physical enrichment for "mature" thymocytes have resulted in the identification of a novel subset of T cells carrying both the Ly-6 antigen and PNA receptors. Purification by fluorescence cell sorting of corticosteroid-treated thymocytes, labeled with monoclonal anti-Ly-2.2 antiserum, for phenotypically mature Ly-1+23-lymphocytes causes a concomitant enrichment in the proportion of Ly-6-positive cells, which lack the PNA receptor. The implications of these findings for the maturational pathways within the thymus are discussed.

Adrenal Cortex Hormones↗
PubMedDate not supplied

Estimating aflatoxin in farmers' stock peanut lots by measuring aflatoxin in various peanut-grade components.

Five, 2 kg test samples were taken from each of 120 farmers' stock peanut lots contaminated with aflatoxin. Kernels from each 2 kg sample were divided into the following grade components: sound mature kernels plus sound splits (SMKSS), other kernels (OK), loose shelled kernels (LSK), and damaged kernels (DAM). Kernel mass, aflatoxin mass, and aflatoxin concentration were measured for each of the 2400 component samples. For 120 lots tested, average aflatoxin concentrations in SMKSS, OK, LSK, and DAM components were 235, 2543, 11,775, and 69,775 ng/g, respectively. Aflatoxins in SMKSS, OK, LSK, and DAM components represented 6.9, 7.9, 33.3, and 51.9% of the total aflatoxin mass, respectively. Cumulatively, 3 aflatoxin risk components--OK, LSK, and DAM--accounted for 93.1% of total aflatoxin, but only 18.4% percent of test sample mass. Correlation analysis suggests that the most accurate predictor of aflatoxin concentration in the lot is the cumulative aflatoxin mass in the high 3 risk components OK + LSK + DAM (correlation coefficient, r = 0.996). If the aflatoxin in the combined OK + LSK + DAM components is expressed in concentration units, r decreases to 0.939. Linear regression equations relating aflatoxin in OK + LSK + DAM to aflatoxin concentration in the lot were developed. The cumulative aflatoxin in the OK + LSK + DAM components was not an accurate predictor (r = 0.539) of aflatoxin in the SMKSS component. Statistical analyses of 3 other data sets published previously yielded similar results.

Aflatoxins↗