Post-fire temporal dynamics of plant-pollinator communities in a tropical savanna.

Fire is a major ecological and evolutionary factor promoting biodiversity and maintaining functioning of naturally fire-prone ecosystems. In tropical savannas, plant communities show a set of fire-adapted traits and both flowering and pollination services have the potential to rapidly regenerate after fire, but fire-suppression policies may disrupt this adaptability following potential woody encroachment. Understanding the effects of fire on plant-pollinator interactions are required to advance conservation of biodiversity and ecosystem functioning.

Evaluation of oxidative damage and genotoxicity in populations exposed to arsenic in drinking water from Santa Fe province, Argentina.

The presence of arsenic in the environment is a public health problem. Groundwater of certain regions of Argentina contains arsenic of natural origin in concentrations that exceed the guide level recommended by World Health Organization (WHO, 10 µg/L). Pathologies derived from chronic arsenic consumption justify the planning of human biomonitoring.

Potentially toxic trace elements in the muscle of coastal South American fish: Implications for human consumption and health risk assessment.

Micropogonias furnieri and Urophycis brasiliensis are two coastal demersal fish species distributed in the southwestern Atlantic Ocean. Considering that many coastal areas in the southwestern Atlantic Ocean suffer from anthropogenic pressure, the aim of this study was to assess the level of potentially toxic trace elements (Ag, Al, As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Mo, Ni, Pb, Se, Sr, V and Zn) in the muscle of coastal species, and evaluated the human health risk related to the consumption of muscle. Mercury, inorganic As (As), V, and Se showed a higher contribution to the total THQ.

Discovery and preclinical development of a therapeutically active nanobody-based chimeric antigen receptor targeting human CD22.

Chimeric antigen receptor (CAR) T cell therapies targeting B cell-restricted antigens CD19, CD20, or CD22 can produce potent clinical responses for some B cell malignancies, but relapse remains common. Camelid single-domain antibodies (sdAbs or nanobodies) are smaller, simpler, and easier to recombine than single-chain variable fragments (scFvs) used in most CARs, but fewer sdAb-CARs have been reported. Thus, we sought to identify a therapeutically active sdAb-CAR targeting human CD22.