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meningococcal A conjugate vaccine (MenAfriVac)

✓ Approved

Serum Institute of India Pvt. Ltd. · 细胞治疗 · 细胞治疗

什么是 meningococcal A conjugate vaccine?

meningococcal A conjugate vaccine 是一种细胞治疗,由Serum Institute of India Pvt. Ltd.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MenAfriVac
公司Serum Institute of India Pvt. Ltd.
药物类别细胞治疗, 疫苗
给药途径Injectable (Others), Intramuscular (IM) Injection
状态Approved

治疗适应症

meningococcal A conjugate 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

PubMedThe Journal of adolescent health : official publication of the Society for Adolescent Medicine2026-08-07

Simultaneous Administration of Human Papillomavirus (HPV) Vaccine With Other Recommended Vaccines Among Adolescents Aged 13-17 years, National Immunization Survey-Teen (NIS-Teen), United States, 2023.

Pingali Cassandra C, Yankey David D, Chen Michael M, Elam-Evans Laurie D LD et al.

To investigate the percent of adolescents who receive human papillomavirus (HPV) vaccine with one or more other vaccines recommended for adolescents in a single medical visit. Data from the 2023 National Immunization Survey-Teen were analyzed. Timing of receipt of HPV vaccine, tetanus, diphtheria, and acellular pertussis vaccine (Tdap), quadrivalent meningococcal conjugate vaccine (MenACWY), and influenza vaccine was assessed using provider-reported vaccination histories. In 2023, among adolescents aged 13-17 years, 69.5% received HPV vaccine with one or more other vaccines recommended for adolescents in a single medical visit. In addition, 47.8% received specifically HPV vaccine, Tdap, and MenACWY together in a single medical visit. The HPV vaccine is commonly given with other vaccines recommended for adolescents in a single medical visit. These findings demonstrate variation in simultaneous vaccination patterns, suggesting that flexibility in the recommended adolescent vaccination schedule allows for different approaches to vaccination across clinical settings and family preferences while maintaining adherence to the recommended schedule.

PMID 42565767
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PubMedVaccine2026-08-07

The marketing authorization of vaccines is not an exact science: the 20-valent pneumococcal conjugate vaccine (PCV-20) is an example.

De Wals Philippe P

PMID 42561780
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PubMedJournal of leukocyte biology2026-08-07

Neutrophils induce effective antibody responses to the pneumococcal conjugate vaccine by inhibiting regulatory T cells.

Tchalla Essi Y I EYI, Betadpur Anagha A, Khalil Andrew Y AY, Lopez Elena E et al.

Neutrophils are required for production of protective antibodies in response to the pneumococcal conjugate vaccine (PCV), however, the mechanisms behind that are not known. Here, using a mouse model, we found that depletion of neutrophils at the time of vaccination in female mice led to aberrant T cell responses in the spleen resulting in increased regulatory T cells (Tregs) that was accompanied by a dysregulated cytokine environment. We found that following vaccination, neutrophils influx into secondary lymphoid organs and increase expression of T cell engaging/inhibiting markers. When we depleted Tregs in neutrophil deficient mice at the time of vaccination, the opsonic activity of the antibodies and the ability of the sera to protect naïve hosts against pneumococcal infection significantly increased compared to controls. Importantly, we examined responses following PCV administration in human female participants and found that PCV altered neutrophil phenotype. Additionally, in vitro coculture of donor neutrophils with their PBMCs at one week following vaccination resulted in lower percentage and proliferation of FOXP3+ T cells, showing the clinical relevance of this phenotype. This work reveals a new mechanism by which neutrophils ensure protective antibody responses to vaccination by suppressing Tregs.

PMID 42565624
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PubMedThe Pediatric infectious disease journal2026-08-07

Clinical and Economic Burden of Complicated Pneumonia and Invasive Disease due to Streptococcus pneumoniae Serotype 19A in an Ecuadorian Pediatric Reference Hospital.

Salgado-Villalba Elías David ED, Costta-Michuy Ángeles Á, Villalba-Valencia Ximena Del Rosario XDR, Carrasco-Ronquillo María Isabel MI et al.

Serotype 19A has emerged as an important cause of pneumococcal disease following the introduction of the 10-valent pneumococcal conjugate vaccine (PCV10). In this retrospective study of children hospitalized with culture-confirmed invasive pneumococcal disease at an Ecuadorian pediatric reference hospital, among 46 cases, 43 (93%) were serotype 19A, with most presenting as severe complicated pneumonia. The majority had received three PCV10 doses. Penicillin nonsusceptibility was identified in 88% of isolates. Serotype 19A infections were associated with longer hospitalization and higher medical costs, highlighting the substantial burden of complicated pneumonia due to a non-PCV10 serotype.

PMID 42563214
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PubMedVaccine2026-08-07

Clinical features and outcomes of pediatric breakthrough invasive pneumococcal disease (IPD) in vaccinated children in Calgary, Alberta, Canada, 2003-2024.

Doucette Emily J EJ, Ricketson Leah J LJ, Murguía-Favela Luis L, Wright Nicola N et al.

Since the introduction of pneumococcal conjugate vaccines (PCV7 in 2002 and PCV13 in 2010) in Alberta, the overall burden of invasive pneumococcal disease (IPD) in children has declined. However, vaccine-type invasive pneumococcal disease (VT-IPD) continues to occur, including in vaccinated children. The Calgary Area Streptococcus pneumoniae Epidemiology Research (CASPER) study is a prospective, population-based surveillance program capturing all IPD cases in the Calgary area. We compared clinical features and outcomes of 227 vaccinated children (<18 years, ≥2 PCV doses) with IPD between 2003 and 2024. Among these, 44 (19.4%) had breakthrough infection and 183 (80.6%) had non-vaccine-type IPD (NVT-IPD). In multivariable analysis, pneumonia/empyema (OR: 5.9, 95% CI: 2.3-14.6) and IPD between 2018 and 2024 (OR: 4.0, 95% CI: 1.2-13.5) were associated with breakthrough infections, whereas comorbidities were not. Serotypes 3 (included in PCV13) and 19F (included in PCV7 and PCV13) accounted for most breakthrough infections. During the late PCV13 era, over 25% of IPD cases were breakthrough infections. Immunologic evaluation of a subset of children with breakthrough disease was largely unremarkable. Although PCVs remain highly effective overall, serotypes 3 and 19F continue to account for a disproportionate number of breakthrough IPD infections. Breakthrough disease became more common during the later PCV13 era and was associated with pneumonia/empyema but not underlying comorbidities, suggesting serotype specific factors may play a greater role than host susceptibility. Continued surveillance is needed to monitor breakthrough disease and the impact of evolving pneumococcal vaccine programs.

PMID 42561781
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PubMedAsia-Pacific journal of public health2026-08-07

Close contact experiences with invasive meningococcal disease contact tracing: Implications for practice.

Milazzo Adriana A, Giles Lynne C LC, Sathiananthan Manjusha K MK, Hanson-Easey Scott S et al.

The aim of this study was to gain in-depth understanding of the experience of the contact tracing process by close contacts of invasive meningococcal disease (IMD) cases. Close contacts participated in semi-structured interviews. We interviewed 26 close contacts of IMD cases; most presented to a hospital emergency department for antibiotic chemoprophylaxis within 24 hours. They had prior knowledge about IMD but experienced anxiety about contracting it; many believed that the antibiotic prevented them from contracting IMD. Contacts were satisfied with information they received during the initial contact from the health department but were concerned about phone calls from an unidentified phone number being disingenuous. Most did not receive any information at the hospital about antibiotic side effects or its function. Findings from this study have implications for the public health response and management of close contacts recommended in jurisdictional IMD guidelines, for Australia and more broadly internationally.

PMID 42565377
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