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L T Wilson

Publications and source records attributed to L T Wilson.

9 recordsLinked to original sources

The effect on the safety of intravenous immunoglobulin of testing plasma for antibody to hepatitis C.

BACKGROUND: The safety of intravenous immunoglobulin (IGIV), manufactured from units testing negative for antibody to hepatitis C virus (anti-HCV), was investigated. STUDY DESIGN AND METHODS: A study involving five chimpanzees was performed to determine whether the safety of IGIV would be compromised if units of plasma that reacted for anti-HCV were withheld from pools from which IGIV is manufactured. In the first phase of the experiment, two chimpanzees were infused with 25 mL per kg of unprocessed, pooled plasma from 2887 donors who did not react for anti-HCV in single-antigen (c100-3) enzyme-linked immunosorbent assays. In the second phase, each of three chimpanzees was infused with 1000 mg per kg of IGIV manufactured from the same plasma units. The immunoglobulin was made by seven United States-licensed manufacturers, each using its own approved method. Each chimpanzee received an equal dose of each manufacturer's IGIV. RESULTS: The two chimpanzees that received anti-c100-3-nonreactive, unprocessed pooled plasma became infected with HCV. The three chimpanzees infused with IGIV did not show any evidence of infection with HCV 15 months after inoculation. Two of these animals were challenged with human non-A,non-B hepatitis-infectious plasma, and both subsequently showed evidence of HCV infection. CONCLUSION: These studies demonstrate that, as determined by infectivity for chimpanzees, 1) the withholding of plasma units that react for anti-c100-3 from pools from which plasma products are manufactured does not render the source material noninfectious, and 2) the safety of IGIV manufactured from such plasma pools is not compromised by withholding the units that react for anti-c100-3.

Animals

Spatial patterns of Anopheles freeborni and Culex tarsalis (Diptera: Culicidae) larvae in California rice fields.

Spatial patterns of Anopheles freeborni Aitken and Culex tarsalis Coquillett larvae were studied during summer by sampling with a standard mosquito dipper in 104 rice fields in northern California. Culex tarsalis larval abundance was highest initially, then decreased and remained low through late summer. An. freeborni larval abundance was low initially, increased steadily, and peaked in mid-August. The degree of aggregation for both species as measured using Taylor's power law and Iwao's Patchiness Regression was highest among the first instars and then decreased as the larvae aged. Seasonal peaks in the degree of aggregation were observed. Analysis of covariance showed that for Taylor's model both instar and time effects were statistically significant, with instar showing the largest effect. In comparison, all slopes resulting from Iwao's model were significantly different, indicating that this model was affected by specific combinations of instar, week, and location and, thus, was less useful in developing an area-wide sampling plan. Optimal sample size was estimated using two methods. One method calculated the number of dips needed to estimate population abundance at three fixed-precision levels. The second calculated the minimum number of dips needed to collect at least one larva. The latter requires a substantially smaller sample size and may provide an effective method for monitoring larval mosquito abundance for control purposes.

Animals

Models for age structured populations with distributed maturation rates.

In the use of age structured population models for agricultural applications such as the modeling of crop-pest interactions it is often essential that the model take into account the distribution in maturation rates present in some or all of the populations. The traditional method for incorporating distributed maturation rates into crop and pest models has been the so-called "distributed delay" method. In this paper we review the application of the distributed delay formalism to the McKendrick equation of an age structured population. We discuss the mathematical properties of the system of ordinary differential equations arising out of the distributed delay formalism. We then discuss an alternative method involving modification of the Leslie matrix.

Aging