The impact of truncating data on the predictive ability for single-step genomic best linear unbiased prediction.

Simulated and swine industry data sets were utilized to assess the impact of removing older data on the predictive ability of selection candidate estimated breeding values (EBV) when using single-step genomic best linear unbiased prediction (ssGBLUP). Simulated data included thirty replicates designed to mimic the structure of swine data sets. For the simulated data, varying amounts of data were truncated based on the number of ancestral generations back from the selection candidates. The swine data sets consisted of phenotypic and genotypic records for three traits across two breeds on animals born from 2003 to 2017. Phenotypes and genotypes were iteratively removed 1 year at a time based on the year an animal was born. For the swine data sets, correlations between corrected phenotypes (Cp) and EBV were used to evaluate the predictive ability on young animals born in 2016-2017. In the simulated data set, keeping data two generations back or greater resulted in no statistical difference (p-value > 0.05) in the reduction in the true breeding value at generation 15 compared to utilizing all available data. Across swine data sets, removing phenotypes from animals born prior to 2011 resulted in a negligible or a slight numerical increase in the correlation between Cp and EBV. Truncating data is a method to alleviate computational issues without negatively impacting the predictive ability of selection candidate EBV.

Engineered immunomodulatory extracellular vesicles derived from epithelial cells acquire capacity for positive and negative T cell co-stimulation in cancer and autoimmunity.

Extracellular vesicles (EVs) are generated by all cells and systemic administration of allogenic EVs derived from epithelial and mesenchymal cells have been shown to be safe, despite carrying an array of functional molecules, including thousands of proteins. To address whether epithelial cells derived EVs can be modified to acquire the capacity to induce immune response, we engineered 293T EVs to harbor the immunomodulatory CD80, OX40L and PD-L1 molecules. We demonstrated abundant levels of these proteins on the engineered cells and EVs. Functionally, the engineered EVs efficiently elicit positive and negative co-stimulation in human and murine T cells. In the setting of cancer and auto-immune hepatitis, the engineered EVs modulate T cell functions and alter disease progression. Moreover, OX40L EVs provide additional benefit to anti-CTLA-4 treatment in melanoma-bearing mice. Our work provides evidence that epithelial cell derived EVs can be engineered to induce immune responses with translational potential to modulate T cell functions in distinct pathological settings.

The impact of selective genotyping on the response to selection using single-step genomic best linear unbiased prediction.

Across the majority livestock species, routinely collected genomic and pedigree information has been incorporated into evaluations using single-step methods. As a result, strategies that reduce genotyping costs without reducing the response to selection are important as they could have substantial economic impacts on breeding programs. Therefore, the objective of the current study was to investigate the impact of selectively genotyping selection candidates on the selection response using simulation. Populations were simulated to mimic the genome and population structure of a swine and cattle population undergoing selection on an index comprised of the estimated breeding values (EBV) for 2 genetically correlated quantitative traits. Ten generations were generated and genotyping began generation 7. Two phenotyping scenarios were simulated that assumed the first trait was recorded early in life on all individuals and the second trait was recorded on all versus a random subset of the individuals. The EBV were generated from a bivariate animal model. Multiple genotyping scenarios were generated that ranged from not genotyping any selection candidates, a proportion of the selection candidates based on either their index value or chosen at random, and genotyping all selection candidates. An interim index value was utilized to decide who to genotype for the selective genotype strategy. The interim value assumed only the first trait was observed and the only genotypic information available was on animals in previous generations. Within each genotyping scenario 25 replicates were generated. Within each genotyping scenario the mean response per generation and the degree to which EBV were inflated/deflated was calculated. Across both species and phenotyping strategies, the plateau of diminishing returns was observed when 60% of the selection candidates with the largest index values were genotyped. When randomly genotyping selection candidates, either 80 or 100% of the selection candidates needed to be genotyped for there not to be a reduction in the index response. Across both populations, no differences in the degree that EBV were inflated/deflated for either trait 1 or 2 were observed between nongenotyped and genotyped animals. The current study has shown that animals can be selectively genotyped in order to optimize the response to selection as a function of the cost to conduct a breeding program using single-step genomic best linear unbiased prediction.