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meningococcal AC/Haemophilus influenzae B type vaccine (Hi Becam / HibACon)

✓ Approved

Chongqing Zhifei Biological · 疫苗 · 疫苗

什么是 meningococcal AC/Haemophilus influenzae B type vaccine?

meningococcal AC/Haemophilus influenzae B type vaccine 是一种疫苗,由Chongqing Zhifei Biological研发。该药已获批,用于治疗相关适应症,给药途径:Injectable (Others)、Intramuscular (IM) Injection。

药物档案

商品名Hi Becam, HibACon
公司Chongqing Zhifei Biological
药物类别疫苗
给药途径Injectable (Others), Intramuscular (IM) Injection
状态Approved

治疗适应症

meningococcal AC/Haemophilus influenzae B type vaccine 针对 1 个适应症,涉及 1 个治疗领域。

治疗领域疾病/病症分期
Infections and infestationsMeningococcal bacteraemia✓ Approved

相关研究文献

PubMedPhysics in medicine and biology2026-06-13

Comparison of four attenuation-compensation methods for backscatter coefficient estimation and characterization of focal liver lesions.

Héroux Arnaud A, Destrempes François F, Rafati Iman I, Barat Maxime M et al.

To compare four attenuation-compensation methods for backscatter coefficient (BSC) estimation, assessment of contrast, and classification of focal liver lesions (FLL). Approach: Ninety-seven patients with 100 FLL were scanned to collect radiofrequency ultrasound images. BSC methods relied on a reference phantom for system and operator-settings independent estimations. Method #1 employed a priori tissue layer segmentation and documented attenuation coefficients (AC) of each layer. Method #2 used a fixed total AC (0.85 dB/cm/MHz). Method #3 used local AC compensation. Method #4 jointly estimated total AC and BSC with a power law frequency model (bf^η). BSC@3MHz, b, η, total AC slope, and total AC were computed within segmented lesions. Lesion contrast was assessed with the contrast-to-noise ratio (CNR) and classification performances were evaluated with the area under the receiver operating characteristic curve (AUC). The composite reference standard was a combination of MRI and histopathology. Main results: The study included 30 primary and 26 secondary cancers, and 44 benign nodules. Parameter b provided the highest CNRs among BSC parameters (p < 0.0001) and gave higher CNRs than B-mode images (p < 0.0001). Method #3 was unsuitable with out-of-range values. Methods #1, #2, and #4 showed no significant differences for b, η, total AC slope, and total AC, whereas BSC@3MHz showed overestimations with Method #4 compared with Methods #1 and #2 (p < 0.001 and p < 0.0001, respectively). For differentiating benign and malignant lesions, η provided the highest AUC of 0.73 (95% confidence interval (CI): 0.62-0.82). For differentiating primary and secondary cancers, BSC@3MHz provided the highest AUC of 0.71 (95% CI: 0.55-0.83). Classification AUCs did not differ between Methods #1, #2 and #4. Significance: BSC imaging improved lesion contrast compared to B-mode and could classify FLL. Method #4 emerged as the most practical as it does not require any a priori AC or segmentation. .

PMID 42285137
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PubMedBMJ (Clinical research ed.)2026-06-13

Meningitis B: UK launches vaccine programme to protect students after fatal outbreaks.

Mahase Elisabeth E

PMID 42285554
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PubMedInfectious diseases (London, England)2026-06-13

Saving the first 24 hours: why public and frontline awareness must accompany meningococcal vaccination.

Nguyen Quynh-Giao QG, Abdullah Rohat Muhyadeen RM, Hassan Eman Fathy Abdeltwab EFA, Dang Van Tri VT et al.

PMID 42286888
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PubMedNature immunology2026-06-13

Human vaccine responses regulated by parallel cytokine pathways.

Chen Guangbo G, Guo Jing J, Heath John J, Prestwood Tyler R TR et al.

Human vaccine responses vary widely, but the determinants remain incompletely defined. Here we analyzed 66 cytokines across four inactivated influenza vaccine (IIV) cohorts over five seasons (n = 581) and identified baseline serum interleukin (IL)-18 and interferon (IFN)-β as correlates of day 28 antibody responses. To test causality, we evaluated 19 cytokines in human tonsil and spleen organoids and found that type I IFNs, IL-21 and IL-12, but not IL-18 or IFNγ, enhanced antibody production. The addition of IFNβ to IIV recapitulated key features of the live-vaccine cytokine program. IL-12 and IL-21 defined a parallel pathway independent of type I IFNs, with IL-12 inducing IL-21 in humans, unlike in mice. Delivery of IL-21 or IFNβ via mRNA lipid nanoparticles in vivo promoted long-lived plasma cell formation. Together, these findings define parallel pathways that regulate vaccine immunity. Our approach unites high-throughput organoid testing and human cohort studies, establishing a human-centric platform to identify adjuvant candidates.

PMID 42286357
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PubMedRevista espanola de anestesiologia y reanimacion2026-06-13

Investigation of dye spread following ultrasound guided injection at the femoral nerve, proximal and distal adductor canal - a cadaver study.

Diwan S S, Mane P P, Gupta A A, Gugapriya T S TS et al.

Total knee arthroplasty (TKA) is associated with significant postoperative pain. Regional analgesic techniques targeting femoral nerve (FN) and adductor canal (AC) are commonly employed; however, uncertainty persists regarding optimal injection site within the AC. Cadaveric investigations provide anatomical insights into injectate spread patterns, but their interpretation requires caution when extrapolating to clinical practice. Twelve thighs from six embalmed human cadavers underwent ultrasound-guided injections of different-colored dyes, with equal volumes administered at three predefined locations: FN, proximal AC, and distal AC. Subsequent anatomical dissections were performed to assess nerve staining patterns. Injection sites and volumes were standardized to allow for comparative anatomical evaluation. Femoral-level injections stained the femoral nerve and its major branches. Proximal AC injections consistently stained both the saphenous nerve and nerve to vastus medialis, whereas distal canal injections predominantly stained the saphenous nerve with only variable distal obturator involvement. The vaso-adductor membrane stained consistently after proximal canal injection. No sciatic nerve staining was observed. Equal-volume dye injections at the FN, proximal AC, and distal AC demonstrate distinct patterns of neural staining. Proximal AC injections resulted in consistent staining of both SN and NVM, whereas distal injections predominantly involved SN. These findings provide anatomical relevance regarding adductor canal block techniques but do not imply clinical superiority of any technique. Clinical correlation is required before extrapolating these observations to clinical practice.

PMID 42285255
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PubMedBMC veterinary research2026-06-13

Proteomics- and immunoinformatics-based design of a multi-epitope vaccine ZZ1 against Glaesserella parasuis.

Wang Zesong Z, Wei Wenbin W, Feng Shifan S, Jia Chaoying C et al.

Glaesserella parasuis (G. parasuis) is a prevalent opportunistic pathogen of the porcine upper respiratory tract, causing substantial economic losses to the global swine industry. Current commercial vaccines exhibit suboptimal heterologous cross-protection and inherent biosafety concerns, highlighting the need for a safe, broadly effective multi-serotype vaccine. This study targeted outer membrane proteins (OMPs) with robust cross-serotype immunogenicity from virulent G. parasuis strains. Comparative proteomic analysis of five strains identified highly abundant, co-expressed OMPs, which were screened based on antigenicity and physicochemical properties. Epitope prediction for helper T lymphocytes (HTL), cytotoxic T lymphocytes (CTL), and B-cells was performed on selected OMPs. Immunodominant epitopes were concatenated using flexible linkers and fused with the TLR2 agonist phenol-soluble modulin α4 (PSMα4) to engineer a multi-epitope vaccine, designated ZZ1. Screening yielded eight conserved OMPs with high antigenicity, hydrophilicity, and thermostability, from which 6 HTL, 7 CTL, and 11 B-cell epitopes were predicted. Immunoinformatic evaluations revealed that ZZ1 possesses a high antigenicity score of 1.018 (threshold: 0.4) and is non-allergenic and non-toxic. Following successful expression, in vivo trials demonstrated that recombinant ZZ1 elicited robust, specific IgG antibody responses. Challenge tests in piglets revealed 100% protective efficacy against G. parasuis serotype 4, and 80% against serotypes 5 and 13. These findings indicate that ZZ1 is a promising candidate capable of conferring broad cross-protection against multiple prevalent G. parasuis serotypes, offering an innovative strategy for next-generation subunit vaccine development.

PMID 42286569
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