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市場調查報告書
商品編碼
1305931
基因載體市場 - 按載體(質粒DNA、腺相關病毒、逆轉錄病毒)、按應用(基因治療、疫苗學)、按疾病(腫瘤、遺傳、感染)、按終端用戶(CDMO、CRO、製藥和生物技術公司),全球預測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,全球基因載體市場規模將顯著擴大。臨床試驗數量的成長將為行業成長鋪平道路。許多臨床試驗都在探索聯合療法的潛力,即基因療法與化療、放療或免疫療法等其他治療方式相結合。這些組合方法通常包括使用多種基因載體來提供不同的治療藥物或增強治療的協同作用。臨床試驗中對聯合療法的探索日益增多,促進了對基因載體的更高需求。
整個基因載體市場根據載體、應用、疾病、終端用戶和地區進行分類。
根據載體,慢病毒細分市場的行業佔有率將在2023年至2032年期間以可觀的年複合成長率成長。基因治療領域不斷增加的投資將為該細分市場的成長帶來有利的機會。慢病毒載體廣泛用作向靶細胞傳遞基因的載體。慢病毒載體可有效地將治療基因等遺傳物質轉移到各種細胞類型中,包括非分裂或緩慢分裂的細胞。這種能力使其在基因治療中具有重要價值,可用於治療遺傳性疾病。
基於疾病,從2023年到2032年,傳染病領域的行業佔有率將以顯著的年複合成長率成長。傳染病的日益流行增加了對基因載體的需求。基因載體可用於開發預防傳染性疾病的疫苗。它們可以將特定的抗原基因傳遞到宿主細胞中,引發免疫反應並產生保護性抗體。這種方法的優勢在於能夠產生廣泛的免疫反應,包括細胞免疫,並具有快速開發新發傳染病疫苗的潛力。
根據終端用戶的不同,到2032年,CRO行業的產值將大幅成長。 CRO數量的增加有助於該細分市場的成長。此外,這些機構在開發基因療法方面的努力進一步推動該細分市場的擴張。 CRO利用基因載體進行臨床前研究,以評估潛在基因療法或基於基因的治療方法的安全性和有效性。
從區域來看,2023年至2032年,亞太地區基因載體市場佔有率將以指數級年複合成長率成長。 HIV/AIDS等傳染性疾病的不斷增加增加了該地區對基因載體的需求。此外,快速發展的醫療基礎設施也進一步促進了該地區的成長。根據IBEF的資料,在2023-24年的聯邦預算中,印度政府向衛生和家庭福利部撥款107.6億美元。
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.