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In the last few years, it has been suggested that the involvement of human leukocyte antigen-G (HLA-G) in several tumoral processes and its likely participation as a factor of immune tolerance in malignant cells. Recently, positive HLA-G surface expression has been associated with a poor prognosis in a small group of patients with B-cell chronic lymphocytic leukemia (B-CLL), a lymphoproliferative disorder characterized by a heterogeneous clinical course. In the present work, 169 patients suffering from B-CLL were analyzed for the expression of HLA-G by flow cytometry in order to verify its prognostic value in a larger cohort. We observed a low expression of this molecule on leukemic B cells and no significant relation to clinical data or progression-free survival time, indicating that this molecule is not as good immunologic prognostic marker for B-CLL as suggested.

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We investigated the alterations of natural killer (NK) cells in pregnancy, which led to decreased killing from the first trimester to the puerperium. We show that this phenomenon cannot be ascribed to a defective number of NK cells since the amounts of HNK-1+, CD16+ (Leu 11), and CD11b+ (OKM1) cells were within normal ranges. Recombinant interleukin 2 (rIL-2) corrects the functional defect in a dose and time-dependent manner, without modification in the surface phenotype of the population. Analysis of the pattern of target cell susceptibility to lysis, together with the similar ability of recombinant interferon gamma (rIFN-gamma) to correct the deficiency, and CD16+, CD3- phenotype of the precursor and effector lymphocytes, demonstrated that the induced cytotoxicity was mediated by NK cells. Inhibitors in pregnancy sera block IL-2 production by specific T cells, but we show that they do not influence either NK activity or its reconstitution by rIL-2. These findings place the deficiency at the level of NK cell maturation into cytotoxic effector lymphocytes. Thus, homeostasis of the NK activity of pregnant women may provide a biological model for clarifying the internal mechanisms regulating NK-cell activation in vivo. Present studies in vitro suggest that modulation of lymphokine production may play a role in the adaptive response of NK cells in pregnancy.

Trophic niche partitioning is a mechanism that facilitates the coexistence of ecologically similar species by sharing their resource use. However, detailed information of the trophic niche in insectivorous birds is usually limited by the lack of accurate identification of consumed food resources. The use of DNA metabarcoding has proved useful for molecular identification of the taxa present in bird faecal samples. Here, we used this molecular technique to study the diets of six steppe passerine species distributed in two Special Protection Areas in central Spain, and to characterize the dietary niche overlap and the prey composition differences between bird species. In total, we distinguished 112 diet items, covering 39 arthropod families of 13 orders. Although significant dietary differences existed in prey species composition, our results indicated a 74% overlap in steppe bird dietary niche, mostly due to high consumption of abundant arthropod prey such as beetles, grasshoppers and spiders in the breeding season by all bird species. The lowest overlap was found for the dietary niches of the Greater Short‐toed Lark Calandrella brachydactyla and Dupont's Lark Chersophilus duponti, a scarce and threatened species, which appeared to be the species with the most distinct dietary niche within the community. Our results make a significant contribution to the knowledge of shrub‐steppe bird diets and their trophic interactions, indicating that some extent of interspecific resource partitioning occurs in the study area, notably between Dupont's Lark and the Greater Short‐toed Lark. Our study demonstrates the value of DNA metabarcoding in the assessment of passerine diets and provides useful ecological results for the design of biodiversity conservation programmes in the increasingly scarce and threatened steppe habitats.