CD25+ T-lymphocytes induce CD11b on eosinophils in allergic nasal mucosa

In the allergic mucosa, there is a significant increase in numbers of CD25+ cells and activated eosinophils. To determine whether a link exists between the activated T-lymphocytes and tissue eosinophils in nasal allergy, we studied CD25+ cells in the nasal mucosa and compared the levels of soluble IL-2 receptor (sIL-2R) both in the serum and the nasal secretions, and further investigated expression of CD11b on eosinophils in the nasal lavage fluids and peripheral blood of patients with nasal allergy. We also examined the effects of the culture supernatant of Con A- and IL-2-activated T-lymphocytes on CD11b expression on eosinophils in the present study. The concentration of sIL-2R in the nasal secretions from patients with Japanese cedar pollinosis (JCP) was significantly higher than that from normal subjects (p < 0.01). The sIL-2R level was significantly higher in the nasal secretions than in the sera in patients (p < 0.01), and CD11b expression on eosinophils from nasal hvage fluid was significandy higher than that of eosinophils from peripheral blood of the same individuals (p < 0.01). The activated T-lymphocytes promoted eosinophil activation with upregulation of CD11b in vitro, and eosinophils in the nasal secretions from patients significantly expressed more CD11b in vivo. These results indicate that activation of T-lymphocytes is linked to eosinophil activation in nasal allergy

CD11/CD18-Dependent and -independent neutrophil emigration in the lungs: How do neutrophils know which route to take?

Neutrophil adhesion to pulmonary microvascular endothelial cells and migration into the distal air spaces of the lungs occur through at least two adhesion pathways: one that requires the leukocyte adhesion complex, CD11/CD18, and one that does not (1–10). Which pathway is selected appears to depend on the stimulus. The role of CD11/CD18 has been primarily established through the use of antibodies to block the function of this molecule. Neutrophil emigration in response to Escherichia coli, E. coli lipopolysaccharide (LPS), Pseudomonas aeruginosa, immunoglobulin (Ig)G immune complexes, interleukin (IL)-1, and phorbol myristate acetate occurs through adhesion pathways that require CD11/CD18 (1–7). In contrast, Streptococcus pneumoniae, Group B Streptococcus, Staphylococcus aureus, hyperoxia, C5a, and hydrochloric acid elicit neutrophil emigration through pathways not inhibited, despite blockade of the CD11/CD18 adhesion complex (1–10). Even when stimuli elicit emigration primarily through CD18-dependent pathways, anti-CD18 antibodies block neutrophil emigration by only 60 to 80%, leaving about 20 to 40% of neutrophils emigrating through CD18-independent pathways. An autopsy report of a child with complete deficiency of CD11/CD18 (leukocyte adhesion deficiency, type I) showed neutrophils and monocytes within the alveoli and small airways (11), suggesting that human neutrophils, as well as those of mice and rats, can use CD11/CD18-independent mechanisms of neutrophil emigration

Very late antigen-4 in CD18-independent neutrophil emigration during acute bacterial pneumonia in mice

This study tested the hypothesis that very late antigen (VLA)-4 mediates CD18-independent neutrophil emigration into the air-spaces induced by either Streptococcus pneumoniae, a stimulus that induces primarily CD18-independent neutrophil emigration, or Escherichia coli, toward which only 20-30% of the total number of neutrophils emigrate through CD18-independent pathways. In wild-type (WT) mice, VLA-4 expression was less on neutrophils that emigrated into the airspaces than on circulating neutrophils. Vascular cell adhesion molecule-1 (VCAM-1) mRNA, the major endothelial cell ligand for VLA-4, increased more in E. coli than in S. pneumoniae pneumonia. VCAM-1 protein expression was not detected in capillaries, the major site of neutrophil emigration. Neutrophil emigration during E. coli or S. pneumoniae pneumonia was similar in mice given antibodies against both CD18 and VLA-4 compared with mice given the anti-CD18 antibody and a control antibody. However, in hematopoietically reconstituted mice with both WT and CD18-deficient neutrophils in their blood, the migration of CD18-deficient neutrophils in response to S. pneumoniae was slightly but significantly less in animals pretreated with the anti-VLA-4 antibody than in those receiving a control antibody. These data suggest that VLA-4 plays a small role in CD18-independent neutrophil emigration, but the majority of CD18-independent neutrophil emigration induced by bacteria in the lungs occurs through VLA-4-independent mechanisms

Search for exotic neutrino-electron interactions using solar neutrinos in XMASS-I

We have searched for exotic neutrino-electron interactions that could be produced by a neutrino millicharge, by a neutrino magnetic moment, or by dark photons using solar neutrinos in the XMASS-I liquid xenon detector. We observed no significant signals in 711 days of data. We obtain an upper limit for neutrino millicharge of 5.4$\times$10$^{-12} e$ at 90\% confidence level assuming all three species of neutrino have common millicharge. We also set flavor dependent limits assuming the respective neutrino flavor is the only one carrying a millicharge, $7.3 \times 10^{-12} e$ for $\nu_e$, $1.1 \times 10^{-11} e$ for $\nu_{\mu}$, and $1.1 \times 10^{-11} e$ for $\nu_{\tau}$. These limits are the most stringent yet obtained from direct measurements. We also obtain an upper limit for the neutrino magnetic moment of 1.8$\times$10$^{-10}$ Bohr magnetons. In addition, we obtain upper limits for the coupling constant of dark photons in the $U(1)_{B-L}$ model of 1.3$\times$10$^{-6}$ if the dark photon mass is 1$\times 10^{-3}$ MeV$/c^{2}$, and 8.8$\times$10$^{-5}$ if it is 10 MeV$/c^{2}$

Search for two-neutrino double electron capture on 124^{124}Xe with the XMASS-I detector

Double electron capture is a rare nuclear decay process in which two orbital electrons are captured simultaneously in the same nucleus. Measurement of its two-neutrino mode would provide a new reference for the calculation of nuclear matrix elements whereas observation of its neutrinoless mode would demonstrate lepton number violation. A search for two-neutrino double electron capture on $^{124}$Xe is performed using 165.9 days of data collected with the XMASS-I liquid xenon detector. No significant excess above background was observed and we set a lower limit on the half-life as $4.7 \times 10^{21}$ years at 90% confidence level. The obtained limit has ruled out parts of some theoretical expectations. We obtain a lower limit on the $^{126}$Xe two-neutrino double electron capture half-life of $4.3 \times 10^{21}$ years at 90% confidence level as well.Comment: 6 pages, 3 figures, accepted for publication in Physics Letters