Usefulness of open data to determine the incidence of COVID-19 and its relationship with atmospheric variables in Spain during the 2020 lockdown.

The SARS-CoV-2 pandemic and the spread of the COVID-19 disease led to a lockdown being imposed in Spain to minimise contagion from 16 March 2020 to 1 May 2020. Over this period, measures were taken to reduce population mobility (a key factor in disease transmission). The scenario thus created enabled us to examine the impact of factors other than mobility (in this case, meteorological conditions) on the incidence of the disease, and thus to identify which environmental variables played the biggest role in the pandemic's evolution. Worthy of note, the data required to perform the study was entirely extracted from governmental open data sources. The present work therefore demonstrates the utility of such data to conduct scientific research of interest to society, leading to studies that are also fully reproducible. The results revealed a relationship between temperatures and the spread of COVID-19. The trend was that of a slightly lower disease incidence as the minimum temperature rises, i.e. the lower the minimum temperature, the greater the number of cases. Furthermore, a link was found between the incidence of the disease and other variables, such as altitude and proximity to the sea. There were no indications, however, in the study's data, of a relationship between incidence and precipitation or wind.

Quantification and phenotype of regulatory T cells in rheumatoid arthritis according to disease activity score-28.

Here we studied and characterized different peripheral blood (PB) regulatory T cell (Treg) subsets in rheumatoid arthritis (RA) patients and tested the hypothesis that changes in these cells can be linked to the degree of inflammation and relapsing/remission periods. PB cells were examined from RA subjects (n = 60) with different disease activity score-28 (DAS28) and from healthy controls (n = 40). Frequencies of Treg subsets expressing characteristic membrane antigens, FoxP3 or intracellular cytokines were quantified by flow cytometry. We observed a decrease in the percentages of CD4(+)CD25(high), CD4(+)CD25(int), CD4(+)CD25(int/high)FoxP3(+), CD4(+)CD38(+), CD4(+)CD62L(+), CD8(+)CD25(high)CD45RA(+) and CD8(+)CD25(int)CD45RA(+) T cells in PB of RA patients compared to healthy controls. In addition, we found increased percentages of cells expressing membrane/intracellular regulatory antigens such as OX40 (CD134), CD45RB(low) or CTLA-4 (CD152), and a higher proportion of other T cell subsets including CD4(+)CTLA-4(+), CD4(+)IL10(+), CD4(+)CD25(int)IL10(+), CD4(+)CD25(int) TGFbeta(+), CD4(+)CD25(low) TGFbeta(+) and CD8(+)CD28(- ). We show that most of these changes parallel the intensity of inflammation, with lowest or highest values in patients with moderately/very active disease compared to healthy controls and at times to patients with inactive RA. The balance between these cell subsets and their antigen expression would determine the inflammation levels and could thus be linked to the relapsing/remission periods of the disease.