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市场调查报告书
商品编码
1305931
基因载体市场 - 按载体(质粒DNA、腺相关病毒、逆转录病毒)、按应用(基因治疗、疫苗学)、按疾病(肿瘤、遗传、感染)、按终端用户(CDMO、CRO、制药和生物技术公司),全球预测2023-2032年Gene Vector Market - By Vector (Plasmid DNA, Adeno-Associated Viral, Retroviral), By Application (Gene Therapy, Vaccinology), By Disease (Oncology, Genetic, Infectious) By End-user (CDMO, CRO, Pharma & Biotech Companies), Global Forecast 2023-2032 |
到2032年,全球基因载体市场规模将显著扩大。临床试验数量的增长将为行业增长铺平道路。许多临床试验都在探索联合疗法的潜力,即基因疗法与化疗、放疗或免疫疗法等其他治疗方式相结合。这些组合方法通常涉及使用多种基因载体来提供不同的治疗药物或增强治疗的协同作用。临床试验中对联合疗法的探索日益增多,促进了对基因载体的更高需求。
整个基因载体市场根据载体、应用、疾病、终端用户和地区进行分类。
根据载体,慢病毒细分市场的行业份额将在2023年至2032年期间以可观的复合年增长率增长。基因治疗领域不断增加的投资将为该细分市场的增长带来有利可图的机会。慢病毒载体被广泛用作向靶细胞传递基因的载体。慢病毒载体可有效地将治疗基因等遗传物质转移到各种细胞类型中,包括非分裂或缓慢分裂的细胞。这种能力使其在基因治疗中具有重要价值,可用于治疗遗传性疾病。
基于疾病,从2023年到2032年,传染病领域的行业份额将以显著的复合年增长率增长。传染病的日益流行增加了对基因载体的需求。基因载体可用于开发预防传染性疾病的疫苗。它们可以将特定的抗原基因传递到宿主细胞中,引发免疫反应并产生保护性抗体。这种方法的优势在于能够产生广泛的免疫反应,包括细胞免疫,并具有快速开发新发传染病疫苗的潜力。
根据终端用户的不同,到2032年,CRO行业的产值将大幅增长。CRO数量的增加有助于该细分市场的增长。此外,这些机构在开发基因疗法方面的努力正在进一步推动该细分市场的扩张。CRO利用基因载体进行临床前研究,以评估潜在基因疗法或基于基因的治疗方法的安全性和有效性。
从区域来看,2023年至2032年,亚太地区基因载体市场份额将以指数级复合年增长率增长。HIV/AIDS等传染性疾病的不断增加增加了该地区对基因载体的需求。此外,快速发展的医疗基础设施也进一步促进了该地区的增长。根据IBEF的数据,在2023-24年的联邦预算中,印度政府向卫生和家庭福利部拨款107.6亿美元。
Global Gene Vector Market size will expand considerably through 2032. Growing number of clinical trials will pave the way for industry growth. Many clinical trials explore the potential of combination therapies, where gene therapy is combined with other treatment modalities such as chemotherapy, radiation therapy, or immunotherapy. These combination approaches often involve the use of multiple gene vectors to deliver different therapeutic agents or enhance treatment synergies. The increasing exploration of combination therapies in clinical trials contributes to the higher demand for gene vectors.
The overall gene vector market is classified based on vector, application, diseases, end-user, and region.
Based on the vector, industry share from the lentiviral segment will grow at a substantial CAGR from 2023 to 2032. Increasing investment in gene therapy will generate lucrative opportunities for segment growth. Lentiviral vectors are widely used as vehicles for delivering genes into target cells. They can efficiently transfer genetic material, such as therapeutic genes, to a range of cell types, including non-dividing or slowly dividing cells. This ability makes them valuable in gene therapy, where they are used to treat genetic disorders.
Based on diseases, industry share from the infectious disease segment will grow at a significant CAGR from 2023 to 2032. Growing prevalence of infectious diseases has increased the demand for gene vectors. Gene vectors can be used to develop vaccines against infectious diseases. They can deliver specific antigen genes into host cells, triggering an immune response and the production of protective antibodies. This approach offers advantages such as the ability to generate a broad immune response, including cellular immunity, and the potential to rapidly develop vaccines for emerging infectious diseases.
Based on the end-user, industry value from the CROs segment will register significant gains through 2032. Increasing number of CROs is contributing to segment growth. Moreover, rising efforts by these organizations toward the development of gene therapies are further creating a notable impetus for segment expansion. CROs conduct preclinical studies using gene vectors to assess the safety and efficacy of potential gene therapies or gene-based treatments.
Regionally, the Asia Pacific gene vector market share will grow at an exponential CAGR from 2023 to 2032. Growing occurrence of infectious disorders such as HIV/AIDS has increased the demand for gene vectors in the region. Moreover, rapidly expanding healthcare infrastructure is further contributing to regional growth. As per IBEF, in the Union Budget 2023-24, the government of India awarded USD 10.76 billion to the Ministry of Health and Family Welfare.