Bioclimatic Characterisation of Specific Native Californian Pinales and Their Future Suitability under Climate Change.

Rising temperatures and changes in precipitation patterns under climate change scenarios are accelerating the depletion of soil moisture and increasing the risk of drought, disrupting the conditions that many plant species need to survive. This study aims to establish the bioclimatic characterisation, both qualitative and quantitative, of ten native Californian Pinales for the period 1980-2019, and to determine their habitat suitability by 2050. To achieve this, an exhaustive search of the Gbif database for records of ten conifer taxa was carried out. To conduct the bioclimatic characterisation of the studied taxa, we worked with the monthly values of average temperature and precipitation for the period 1980-2019 from 177 meteorological stations. Linear regressions was performed in order to compile the future evolution of California's climate. Suitable areas and optimal areas were defined at the present time (1980-2019) and its future projection (2050). We applied Boolean logic and, in this investigation, the Conditional Logic Operator (CON) was used to determine the possible species presence (one) or absence (zero) for each of the 15 variables analysed. In general, most of the conifers studied here will experience a reduction in their habitat range in California by the year 2050 due to climate change, as well as the displacement of species towards optimal areas. Furthermore, the results have highlighted the applicability of bioclimatology to future conditions under climate change. This will aid conservation managers in implementing strategic measures to ameliorate the detrimental impacts of climate change, thereby ensuring the ecological integrity and sustainability of the affected conifer species.

Genetic deletion of HVEM in a leukemia B cell line promotes a preferential increase of PD-1- stem cell-like T cells over PD-1+ T cells curbing tumor progression.

Introduction: A high frequency of mutations affecting the gene encoding Herpes Virus Entry Mediator (HVEM, TNFRSF14) is a common clinical finding in a wide variety of human tumors, including those of hematological origin. Methods: We have addressed how HVEM expression on A20 leukemia cells influences tumor survival and its involvement in the modulation of the anti-tumor immune responses in a parental into F1 mouse tumor model of hybrid resistance by knocking-out HVEM expression. HVEM WT or HVEM KO leukemia cells were then injected intravenously into semiallogeneic F1 recipients and the extent of tumor dissemination was evaluated. Results: The loss of HVEM expression on A20 leukemia cells led to a significant increase of lymphoid and myeloid tumor cell infiltration curbing tumor progression. NK cells and to a lesser extent NKT cells and monocytes were the predominant innate populations contributing to the global increase of immune infiltrates in HVEM KO tumors compared to that present in HVEM KO tumors. In the overall increase of the adaptive T cell immune infiltrates, the stem cell-like PD-1- T cells progenitors and the effector T cell populations derived from them were more prominently present than terminally differentiated PD-1+ T cells. Conclusions: These results suggest that the PD-1- T cell subpopulation is likely to be a more relevant contributor to tumor rejection than the PD-1+ T cell subpopulation. These findings highlight the role of co-inhibitory signals delivered by HVEM upon engagement of BTLA on T cells and NK cells, placing HVEM/BTLA interaction in the spotlight as a novel immune checkpoint for the reinforcement of the anti-tumor responses in malignancies of hematopoietic origin.