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AP

aP vaccine (aP vaccine, NAVA)

✓ Approved

Baxter International, Inc. · 疫苗 · 疫苗

什么是 aP vaccine?

aP vaccine 是一种疫苗,由Baxter International, Inc.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aP vaccine, NAVA
公司Baxter International, Inc.
药物类别疫苗
给药途径Injectable (Others), Intramuscular (IM) Injection
状态Approved

治疗适应症

aP 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 infestationsPertussis✓ Approved

相关研究文献

PubMedCureus2026-10-26

Non-invasive Neurally Adjusted Ventilatory Assist (NIV-Nava): Four-Year Experience in a Level III Neonatal Intensive Care Unit.

Ferreira Madalena M, Roquette Margarida M, Belo Inês I, Correia Cátia R CR et al.

Introduction Non-invasive neurally adjusted ventilatory assist (NIV-NAVA) is a ventilation mode that uses the electrical activity of the diaphragm to synchronize respiratory support with the patient's spontaneous effort. It has emerged as a promising non-invasive modality for neonates. We aimed to evaluate the clinical success of NIV-NAVA in a neonatal intensive care unit (NICU) setting. To our knowledge, this is the first study in Portugal to describe the experience with NIV-NAVA in a level III NICU. Methods We conducted an observational retrospective cohort study through a medical record review over four years (January 2021 to December 2024). All newborns admitted to our NICU who were ventilated using NIV-NAVA were included. Descriptive statistical analysis was performed on demographic and diagnostic data. Ventilatory and gasometrical parameters, including fraction of inspired oxygen (FiO₂), pH, and partial pressure of carbon dioxide (pCO₂), were evaluated before and after NIV-NAVA initiation. A respiratory severity score (RSS) was calculated at baseline to assess the severity of respiratory disease. The primary outcome was the proportion of NIV-NAVA episodes not requiring subsequent endotracheal intubation, and success was defined as the avoidance of subsequent intubation. Results A total of 36 NIV-NAVA episodes were recorded across 28 newborns, with a mean gestational age of 26 weeks and a mean birth weight of 822g. All newborns were diagnosed with prematurity, respiratory distress syndrome, and bronchopulmonary dysplasia. The mean baseline RSS was 3.7, reflecting the respiratory disease burden at NIV-NAVA initiation. NIV-NAVA was initiated following extubation in 83.3% of cases and as therapeutic escalation in 16.7%. Success was achieved in 58.3% of all episodes (60% in the post-extubation group and 50% in the escalation group). No statistically significant differences were observed in mean FiO₂ or pCO₂ values before and after NIV-NAVA. Discussion NIV-NAVA success was observed in the majority of newborns, including extremely low birth weight infants with clinically relevant respiratory disease burden. While NIV-NAVA offers significant theoretical advantages regarding patient-ventilator synchronization, published evidence in the NICU remains limited. Conclusion Our findings support the use of NIV-NAVA as a feasible non-invasive ventilatory modality in preterm infants, particularly for post-extubation respiratory support, although further randomized controlled trials are warranted to better establish its role and efficacy within the neonatal population.

PMID 42928955
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PubMedGels (Basel, Switzerland)2026-10-26

Ambient-Dried Cellulose Nanofibril/H2TiO3 Composite Aerogel for Enhanced Lithium Capture at Seawater-Relevant pH.

Wang Xueqiao X, Wang Jing J, Wang Wenxuan W, Liu Ruimeng R et al.

Efficient seawater lithium harvesting requires adsorbents combining high selectivity with scalable, low-energy fabrication. Although H2TiO3 lithium-ion sieves (HTO-LIS) exhibit exceptional Li+ selectivity, their deployment is hindered by strict alkaline requirements and reliance on energy-intensive shaping processes such as freeze-drying. Herein, we report a cellulose nanofibril (CNF) composite aerogel addressing both challenges simultaneously. Ammonium phytate (AP), a bio-derived polyphosphate, serves a dual function: as a green crosslinker for CNF and as an in situ alkalinity generator, creating a localized alkaline microenvironment around immobilized HTO nanoparticles that enables efficient topotactic H+/Li+ exchange at seawater-relevant pH 8 without requiring strongly alkaline bulk conditions. Crucially, the AP-crosslinked CNF skeleton withstands capillary forces during ambient-pressure drying, preserving a hierarchical macroporous network without freeze-drying. The resulting AP-CNF@HTO monolith achieves a Li+ capacity of 19.08 mg g-1 at pH 8, a 128.9% enhancement over pristine HTO, with excellent selectivity against competing ions in real seawater and 88.3% capacity retention after ten cycles. This work demonstrates that rational bio-based crosslinker selection can concurrently solve the alkaline microenvironment and ambient-drying challenges of HTO-LIS composites, offering an ambient-pressure-drying route with reduced reliance on energy-intensive freeze-drying for seawater lithium enrichment.

PMID 42929908
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PubMedCancer discovery2026-10-26

First mRNA Cancer Vaccine Succeeds in Phase III Trial.

Adding the mRNA-based individualized neoantigen vaccine intismeran autogene to the PD-1 inhibitor pembrolizumab following surgery for melanoma reduced the risk of disease recurrence or death by 42%, according to the results of the phase III INTerpath-0001 trial. The data were presented at the ESMO Congress 2026, held October 23-27, in Madrid, Spain.

PMID 42929716
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PubMedAnimal health research reviews2026-10-26

Innovative vaccine strategies for sustainable control and eradication of peste des petits ruminants virus.

Bello Muhammad Bashir MB, Hameed Sodiq A SA, Abdullahi Adama Musa AM, Lawal Nafi'u N et al.

PMID 42929676
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PubMedEpidemiologia (Basel, Switzerland)2026-10-26

A Carriage-Structured Model of Meningococcal Meningitis: Backward Bifurcation, Seasonal Recurrence, and the Reach of Conjugate-Vaccine Strategies in the African Meningitis Belt.

Gatyeni Siphokazi Princess SP

Epidemic meningococcal meningitis in the African meningitis belt recurs on two timescales: a sharp annual dry-season peak and irregular multi-annual epidemics five to twelve years apart, whose mechanistic origin remains unsettled. Invasive disease is a rare, dead-end outcome of asymptomatic nasopharyngeal carriage, so susceptible-infectious templates misrepresent community transmission. We ask how carriage structure shapes bifurcation, seasonal recurrence, and the reach of conjugate-vaccine strategies. We formulate a deterministic carriage-structured model in which only carriers transmit, immunity against re-acquisition is leaky, and a conjugate vaccine is imperfect and wanes. We use the Castillo-Chavez-Song centre manifold method, numerical continuation, Floquet and eigenvalue analysis, and scenario simulations of abstract rate- and pulse-type interventions parameterised from published belt ranges. The basic reproduction number R0 is a property of carriage transmission, decoupled to first order from disease incidence. Backward bifurcation at R0=1 is governed by a threshold ε∗ on carriage-blocking immunity; only the untreated fatality hazard and treatment capacity are absent from the local condition. It is impossible without vaccination and, with any positive routine coverage, persists across the plausible coverage range, giving vaccine-induced bistability. Continuation confirms a fold at R0,c≈0.946 (φ=0.12yr-1, weak carriage immunity), but not at baseline immunity. Under seasonal forcing, dynamics converge to a simple annual cycle throughout the region searched; we found no multi-annual recurrence, although damped eigenmodes of the unforced system have periods overlapping the observed interval. Within this deterministic, single-strain model, irregular recurrence likely requires additional structure, with stochastic amplification of damped cycles a natural next step. Whether sustained immunisation eliminates epidemics or merely postpones them may depend on the same carriage-efficacy threshold that governs the bistability result.

PMID 42930328
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PubMedJournal of virology2026-10-26

Early innate immune signatures correlate with Ad26.COV2.S vaccine immunogenicity and protective efficacy.

Colarusso Alessandro A, Stephenson Kathryn E KE, Collier Ai-Ris Y A-RY, Wegmann Frank F et al.

The innate immune system is rapidly activated following antigen exposure and plays a critical role in shaping the ensuing adaptive immune responses. In this study, we performed bulk RNA sequencing and proteomic profiling in a cohort of 25 rhesus macaques following Ad26.COV2.S immunization to characterize early innate correlates of vaccine immunogenicity and protection. Our results show that innate immune activation occurred as early as day 1 post-vaccination and demonstrated a systemic enrichment of antiviral interferon pathways, cytokine signaling, and activation of innate immune cell signatures. These early transcriptomic signatures correlated positively with humoral and cellular immune responses at 6 weeks following vaccination and correlated inversely with viral loads following SARS-CoV-2 challenge. Similar correlates of immunogenicity were observed in a cohort of 25 adult healthy participants vaccinated with Ad26.COV2.S. Taken together, these findings highlight the importance of early activation of the innate immune responses following Ad26.COV2.S vaccination in shaping the protective adaptive immune response.IMPORTANCEEarly innate immune responses may shape vaccine immunogenicity and protection. We evaluated responses to Ad26.COV2.S vaccination in rhesus macaques and humans and found that day 1 innate immune signatures correlated with subsequent adaptive responses. These findings suggest that early post-vaccination immune programming influences immunogenicity and protective efficacy months later.

PMID 42929544
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