Trivalent Groups Research Articles

The innate immune response following multivalent dengue vaccination and implications for protection against dengue challenge.

Understanding the immune response to dengue virus (DENV) is essential for developing a dengue vaccine that is protective against all 4 DENV serotypes. We evaluated the immune response after vaccination (live attenuated tetravalent dengue vaccine TV005 or trivalent admixture) and after challenge with DEN2Δ30 (Tonga/74) to better understand the importance of homotypic immunity in vaccine protection. Significant increases in IP-10 expression were observed following receipt of either the trivalent or tetravalent vaccine. After challenge, a large increase in IP-10 expression was observed in the placebo and trivalent admixture groups but not in the tetravalent vaccine group. MCP-1, IL-1RA, and MIP-1β exhibited a similar pattern as IP-10. These results demonstrate protective effects of trivalent and tetravalent vaccines against DENV and suggest that the tetravalent vaccine has a better protective effect compared with the trivalent admixture. We also explored the postvaccination and postchallenge immune response differences between Black and White participants. White participants responded to vaccine differently than Black participants; Black participants receiving trivalent and tetravalent vaccines responded strongly and White participants responded only transiently in trivalent group. In response to challenge, White participants elicited a stronger response than Black participants. These results may explain why White participants may have a more vigorous DENV immune response than Black participants, as reported in literature.

Photoinduced Bisphosphination of Alkynes with Phosphorus Interelement Compounds and Its Application to Double-Bond Isomerization.

The addition of interelement compounds with heteroatom-heteroatom single bonds to carbon-carbon unsaturated bonds under light irradiation is believed to be an atomically efficient method to procure materials with carbon-heteroatom bonds. In this study, we achieved the photoinduced bisphosphination of alkynes using the phosphorus interelement compound, tetraphenyldiphosphine monosulfide (1), to stereoselectively obtain the corresponding (E)-vic-1,2-bisphosphinoalkenes, which are important transition-metal ligands. The bisphosphination reaction was performed by mixing 1 and various alkynes and then exposing the mixture to light irradiation. Optimization of the conditions for the bisphosphination reaction resulted in a wide substrate range and excellent trans-selectivity. Moreover, the completely regioselective introduction of pentavalent and trivalent phosphorus groups to the terminal and internal positions of the alkynes, respectively, was achieved. We also found that the novel double-bond isomerization reaction of the synthesized bisphosphinated products occurred with a catalytic amount of a base under mild conditions. Our method for the photoinduced bisphosphination of carbon-carbon unsaturated compounds may have strong implications for both organic synthesis and organometallic and catalyst chemistry.

Safety and immunogenicity of two heterologous HIV vaccine regimens in healthy, HIV-uninfected adults (TRAVERSE): a randomised, parallel-group, placebo-controlled, double-blind, phase 1/2a study

SummaryBackgroundBioinformatically designed mosaic antigens increase the breadth of HIV vaccine-elicited immunity. This study compared the safety, tolerability, and immunogenicity of a newly developed, tetravalent Ad26 vaccine with the previously tested trivalent formulation.MethodsThis randomised, parallel-group, placebo-controlled, double-blind, phase 1/2a study (TRAVERSE) was done at 11 centres in the USA and one centre in Rwanda. Eligible participants were adults aged 18 to 50 years, who were HIV-uninfected, healthy at screening based on their medical history and a physical examination including laboratory assessment and vital sign measurements, and at low risk of HIV infection in the opinion of study staff, who applied a uniform definition of low-risk guidelines that was aligned across sites. Enrolled participants were randomly assigned at a 2:1 ratio to tetravalent and trivalent groups. Participants in tetravalent and trivalent groups were then further randomly assigned at a 5:1 ratio to adenovirus 26 (Ad26)-vectored vaccine and placebo subgroups. Randomisation was stratified by region (USA and Rwanda) and based on a computer-generated schedule using randomly permuted blocks prepared under the sponsor's supervision. We masked participants and investigators to treatment allocation throughout the study. On day 0, participants received a first injection of tetravalent vaccine (Ad26.Mos4.HIV or placebo) or trivalent vaccine (Ad26.Mos.HIV or placebo), and those injections were repeated 12 weeks later. At week 24, vaccine groups received a third dose of tetravalent or trivalent together with clade C gp140, and this was repeated at week 48, with placebos again administered to the placebo group. All study vaccines and placebo were administered by intramuscular injection in the deltoid muscle. We assessed adverse events in all participants who received at least one study injection (full analysis set) and Env-specific binding antibodies in all participants who received at least the first three vaccinations according to the protocol-specified vaccination schedule, had at least one measured post-dose blood sample collected, and were not diagnosed with HIV during the study (per-protocol set). This study is registered with Clinicaltrials.gov, NCT02788045.FindingsOf 201 participants who were enrolled and randomly assigned, 198 received the first vaccination: 110 were in the tetravalent group, 55 in the trivalent group, and 33 in the placebo group. Overall, 185 (93%) completed two scheduled vaccinations per protocol, 180 (91%) completed three, and 164 (83%) completed four. Solicited, self-limiting local, systemic reactogenicity and unsolicited adverse events were similar in vaccine groups and higher than in placebo groups. All participants in the per-protocol set developed clade C Env binding antibodies after the second vaccination, with higher total IgG titres after the tetravalent vaccine than after the trivalent vaccine (10 413 EU/mL, 95% CI 7284–14 886 in the tetravalent group compared with 5494 EU/mL, 3759–8029 in the trivalent group). Titres further increased after the third and fourth vaccinations, persisting at least through week 72. Other immune responses were also higher with the tetravalent vaccine, including the magnitude and breadth of binding antibodies against a cross-clade panel of Env antigens, and the magnitude of IFNγ ELISPOT responses (median 521 SFU/106 peripheral blood mononuclear cells [PBMCs] in the tetravalent group and median 282 SFU/106 PBMCs in the trivalent group after the fourth vaccination) and Env-specific CD4+ T-cell response rates after the third and fourth vaccinations. No interference by pre-existing Ad26 immunity was identified.InterpretationThe tetravalent vaccine regimen was generally safe, well-tolerated, and found to elicit higher immune responses than the trivalent regimen. Regimens that use this tetravalent vaccine component are being advanced into field trials to assess efficacy against HIV-1 infection.FundingNational Institutes of Health, Henry M Jackson Foundation for Advancement of Military Medicine and the US Department of Defense, Ragon Institute of MGH, MIT, & Harvard, Bill & Melinda Gates Foundation, and Janssen Vaccines & Prevention.

Influence of gut microbiota on mucosal IgA antibody response to the polio vaccine

The impact of intestinal microbiota on mucosal antibody response to the polio vaccine is poorly understood. We examined changes in vaccine-induced intestinal mucosal immunity to poliovirus by measuring the immunoglobulin A (IgA) antibody levels in stool samples collected from 107 infants in China, and the samples were collected 14 days after different sequential vaccinations combining inactivated polio vaccine (IPV) with oral poliovirus vaccine (OPV). Gut microbiota were identified using 16S ribosomal RNA sequencing 28 days before, 14 days before, and at the last dose of OPV. Vaccine-induced type 2-specific mucosal IgA showed a decrease after switching from trivalent to bivalent OPV (bOPV) (positive rate of polio type 2-specific mucosal IgA, 16.7%, 11.8%, and 45.9% for IPV + 2bOPV, 2IPV + bOPV, and 2IPV + trivalent OPV groups, respectively). The composition of the gut microbiome was significantly different, a higher abundance of Firmicutes and a lower abundance of Actinobacteria were observed in IgA-negative infant (n = 66) compared with IgA-positive infants (n = 39), and the gut microbiota were more diverse in IgA-negative infants on the day of OPV inoculation. The abundance of Clostridia was concomitant with a significantly lower conversion rate of mucosal IgA responses to the polio vaccine. The composition of the gut microbiome may affect the intestinal mucosal IgA response to the polio vaccine.

Structural, spectroscopic and computational examination of the dative interaction in constrained phosphine-stibines and phosphine-stiboranes.

A series of phosphine-stibine and phosphine-stiborane peri-substituted acenaphthenes containing all permutations of pentavalent groups -SbCln Ph4-n (5-9), as well as trivalent groups -SbCl2 , -Sb(R)Cl, and -SbPh2 (2-4, R=Ph, Mes), were synthesised and fully characterised by single crystal diffraction and multinuclear NMR spectroscopy. In addition, the bonding in these species was studied by DFT computational methods. The P-Sb dative interactions in both series range from strongly bonding to non-bonding as the Lewis acidity of the Sb acceptor is decreased. In the pentavalent antimony series, a significant change in the P-Sb distance is observed between -SbClPh3 and -SbCl2 Ph2 derivatives 6 and 7, respectively, consistent with a change from a bonding to a non-bonding interaction in response to relatively small modification in Lewis acidity of the acceptor. In the Sb(III) series, two geometric forms are observed. The P-Sb bond length in the SbCl2 derivative 2 is as expected for a normal (rather than a dative) bond. Rather unexpectedly, the phosphine-stiborane complexes 5-9 represent the first examples of the σ(4) P→σ(6) Sb structural motif.

A polyion complex nanogel

Here, we synthesized dextrans modified with trivalent cationic or anionic groups. Aqueous solutions of the cationic and anionic dextrans were then mixed resulting in the formation of polyion complex nanogels (PIC-NGs), which have physically crosslinked salt bridges formed between the cationic and anionic groups. To prepare PIC-NGs in high yield, the content of ionic groups in the cationic and anionic dextrans should be low to avoid interparticle salt bridge formation. The structure of the PIC-NGs is easily affected by the ionic strength of the solution because of shielding of the charges in the ionic groups. However, the conversion of a small amount of the physical crosslinks to covalent crosslinks significantly improved the stability of the PIC-NGs. The covalent crosslinking also stabilized the PIC-NGs against pH change, which will destabilize the salt bridges. These results indicated that the conversion of the small amount of physical crosslinks to covalent crosslinks stabilized the other salt bridges.

A Facile Approach to Fabricate Self‐Standing Gel‐Polymer Electrolytes for Flexible Lithium‐Ion Batteries by Exploitation of UV‐Cured Trivalent/Monovalent Acrylate Polymer Matrices

AbstractA facile approach to fabricate a self‐standing GPE for flexible lithium‐ion batteries is demonstrated using a UV‐cured trivalent/monovalent acrylate polymer matrix and a liquid electrolyte. The polymer matrix is successfully synthesized with the co‐presence of the liquid electrolyte by UV polymerization of ETPTA, which has trivalent vinyl groups, and EGMEA, which contains monovalent vinyl groups, with the ETPTA/EGMEA ratio fixed at 90/10 (wt%/wt%). The ETPTA/EGMEA matrix shows a lower Tg than the ETPTA matrix alone, which helps improve the mechanical flexibility and ionic transport of the resulting GPE. These features of the ETPTA/EGMEA‐based GPE, together with its superior interfacial compatibility towards electrodes, play crucial roles in obtaining a better cell performance compared to the ETPTA‐based GPE.

Influencing Particle Size and Stability of Ionic Dendrimer−Dye Assemblies

This article focuses on the physical chemical aspects of the formation of supramolecular nanoparticles with defined size and varying shape through electrostatic self-assembly of macroions and multivalent aromatic counterions. For cationic poly(amidoamine) dendrimers and different di- and trivalent sulfonate groups carrying azo dyes, the onset of interdendrimer connection and assembly size (hydrodynamic radius 20 nm < R(h) < 150 nm) depend on counterion/macroion loading ratio. Centrifugation and dialysis experiments show assemblies coexisting with individual dye-loaded dendrimers with lower dye/dendrimer ratio at small loading ratio, while around charge stoichiometry only assemblies are present. Zeta-potential measurements reveal a positive charge for samples with excess dendrimer. For excess dye, overloading to negatively charged assemblies is possible for some dyes, which is consistent with concentration-dependent stability revealing a second mode of more loosely bound dye ions. Kinetic versus thermodynamic effects are discussed based on varying the preparation route. The interaction enthalpy is an important factor in determining assembly size. Solution structures are characterized by static and dynamic light scattering, while atomic force microscopy showed that assemblies can also be deposited on surfaces.

Characterization of a Novel Polyphenol-Specific Oligoxyloside Transfer Reaction by a Family 11 Xylanase fromBacillussp. KT12

A culture filtrate of Bacillus sp. KT12 was used to prepare polyphenyl beta-oligoxylosides from xylan and polyphenols in a one-step reaction. One oligoxyloside transfer enzyme was purified from multiple xylanolytic enzymes in the culture filtrate. N-terminal amino acid sequence determination classified the enzyme as a glycosyl hydrolase family 11 (endo-xylanase). The xylanolytic enzyme activities could be markedly altered; its hydrolytic activity was almost entirely inhibited at acidic pH, whereas near constant transxylosylation activity was observed at pH 4-11. Further, metal ions activated transxylosylation and almost completely inhibited hydrolysis. The enzyme specifically induced a beta-xylosyl transfer reaction to acceptor molecules, such as divalent and trivalent phenolic hydroxyl groups, and displayed no activity toward alcoholic compounds. The Bacillus sp. KT12 xylanolytic enzyme was a suitable enzyme for the synthesis of polyphenyl beta-oligoxylosides.

Hydroxyoligophosphites and -Phosphonites on the Basis of 1,4:3,6-Dianhydro-D-sorbitol

The interaction of 1,4:3,6-dianhydro-D-sorbitol with phosphorous and phenylphosphonous acid amidochlorides leads to oligophosphites and -phosphonites with free hydroxyl groups on the periphery of their molecules. The obtained compounds were introduced into reactions via the transformation of trivalent phosphorus and hydroxyl groups.

The effect of multiple simple Robertsonian heterozygosity on chromosome pairing and fertility of wild-stock house mice (Mus musculus domesticus)

The influence of Robertsonian (Rb) heterozygosity on fertility has been the subject of much study in the house mouse. However, these studies have been largely directed at single simple heterozygotes (heterozygous for a single Rb metacentric) or complex heterozygotes (heterozygous for several to many metacentrics which share common chromosome arms). In this paper we describe studies on male multiple simple heterozygotes, specifically the F₁ products of crosses between wild-stock mice homozygous for four or seven metacentrics and wild-stock mice with a standard all-acrocentric karyotype; these F₁ products were characterized by four and seven trivalents at meiosis I, respectively. Mice with the same karyotype, but two different genetic backgrounds were examined. Although a range of meiotic and fertility studies were conducted, particular emphasis was paid to analysis of chromosome pairing, previously not well-described in multiple simple heterozygous mice. The progression of spermatocytes through prophase I was followed by electron microscopy of surface spread material. As previously shown for single simple Rb heterozygotes, the trivalents that characterize multiple simple heterozygotes initially showed delayed pairing of the centromeric region and later showed side arm formation, resulting from non-homologous pairing by the centromeric ends of the acrocentric chromosomes. In the four trivalent groups of mice, 15 and 32% of trivalents showed unpairing in the centromeric region at mid pachytene; equivalent values were 29 and 39% for the seven trivalent groups. Pairing abnormalities (largely attachments and interlocks between trivalents and between a trivalent and the XY configuration) were observed in 18 and 23% of mid pachytene cells in the four trivalent groups and 36 and 49% of cells in the seven trivalent groups. The greater level of pachytene irregularity (unpairing and pairing abnormalities) in seven versus four trivalent heterozygotes was mirrored in terms of higher anaphase I nondisjunction frequency and lower germ cell counts. However, while pachytene irregularities appear to contribute to germ cell death, examples of male sterility in our material undoubtedly also involve genic incompatibilities.

Phosphorus‐containing groups in analyses of carbon‐13 chemical shifts of 1‐hetera‐4‐cyclohexanones

AbstractThe 13C NMR chemical shifts of a series of phosphorinanes and the corresponding 4‐phosphorinanones have been evaluated using ‘double difference’ plots. Most of the compounds fit the same linear relationships for the carbons alpha and beta to the hetera group previously found for the analogous sulfur, oxygen and nitrogen six‐membered heterocycles, suggesting that these phosphorus compounds possess similar chair conformations. For the carbons gamma to the hetera group, the plots suggest that there are transannular interactions between the trivalent phosphine groups and the carbonyl group, similar to that previously observed for the sulfide group. In these 1‐hetera‐4‐cyclohexanones, transannular interactions appear whenever a lone pair of electrons on a second‐row heteroatom is present in the proper conformation for interaction with the carbonyl group.

Supported transition metal complexes : I. Organic polymers as the slipport

Trivalent phosphorus ligand groups have been bonded to a wide range of organic polymers, including polyvinyl chloride, polystyrene, polybutadiene and polyvinyl alcohol. The ligand-polymers complex with a variety of transition metal compounds, and the complexes obtained have been shown to catalyse hydrocarbon reactions such as the hydrogenation of 1-hexene and cyclohexene, the hydroformylation of 1-hexene and the cyclodimerisation of butadiene to 4-vinylcyclohexene and 1,5-cyclooctadiene. Macroreticular high surface area cross-linked polystyrene is the most satisfactory organic polymer support. Rhodium complexes of acetylacetone ligand-polymers have also been prepared.

Cytological Studies of Lilium tigrinum

1. Development of the megagametophyte in Lilium tigrinum var. splendens follows the general plan reported for the other members of the genus and for Fritillaria and Tulipa. 2. At metaphase of the first meiotic division 36 chromosomes generally occur in 12 trivalent groups, although bivalents and univalents may occur. 3. Distribution of chromosomes at the first meiotic division approaches random assortment, except that there are marked increases toward the 1n and 2n limits of distribution. 4. The chromatids of lagging chromosomes may separate precociously following the first meiotic division, after which they may pass tardily to the poles or remain in the cytoplasm between the two nuclei. 5. Lagging chromosomes and fragments eliminated from nuclei may disintegrate or persist as micronuclei. 6. Elimination of chromosomes through lagging and fragmentation in the meiotic divisions and to a less marked degree in the divisions following meiosis produces a general shift in the distribution toward the lower chromosome numbers. 7. Lagging chromosomes and bridging occur in the divisions following meiosis in the development of the megagametophyte. 8. The occurrence of chromatid bridges and fragmentation of chromosomes at meiosis results from crossing-over in an inverted segment of one of the chromosomes. 9. Crossing-over in an inversion results in the formation of dicentric chromosomes at meiosis in a triploid and thus favors the formation of haploid and diploid gametes. 10. There is close parallelism between meiotic irregularities found in structural hybrids and irregularities common to triploids.

On the Quantum Mechanical Stability of a Benzol Molecule

The Heitler-London-Rumer treatment of valence bonds is applied to the benzol molecule, considered as a system of six trivalent nitrogen-like CH groups. Partial solution of the secular equation of the thirty-fourth degree shows that this model of the benzol ring is thermodynamically unstable relative to three acetylene molecules, in disagreement with experiment. The method does not take cognizance of the directional properties of valence bonds (Slater-Pauling).