Combination of AAV-delivered tumor suppressor PTEN with anti-PD-1 loaded depot gel for enhanced antitumor immunity
© 2024 The Authors..
Recent clinical studies have shown that mutation of phosphatase and tensin homolog deleted on chromosome 10 (PTEN) gene in cancer cells may be associated with immunosuppressive tumor microenvironment (TME) and poor response to immune checkpoint blockade (ICB) therapy. Therefore, efficiently restoring PTEN gene expression in cancer cells is critical to improving the responding rate to ICB therapy. Here, we screened an adeno-associated virus (AAV) capsid for efficient PTEN gene delivery into B16F10 tumor cells. We demonstrated that intratumorally injected AAV6-PTEN successfully restored the tumor cell PTEN gene expression and effectively inhibited tumor progression by inducing tumor cell immunogenic cell death (ICD) and increasing immune cell infiltration. Moreover, we developed an anti-PD-1 loaded phospholipid-based phase separation gel (PPSG), which formed an in situ depot and sustainably release anti-PD-1 drugs within 42 days in vivo. In order to effectively inhibit the recurrence of melanoma, we further applied a triple therapy based on AAV6-PTEN, PPSGanti-PD-1 and CpG, and showed that this triple therapy strategy enhanced the synergistic antitumor immune effect and also induced robust immune memory, which completely rejected tumor recurrence. We anticipate that this triple therapy could be used as a new tumor combination therapy with stronger immune activation capacity and tumor inhibition efficacy.
Medienart: |
E-Artikel |
---|
Erscheinungsjahr: |
2024 |
---|---|
Erschienen: |
2024 |
Enthalten in: |
Zur Gesamtaufnahme - volume:14 |
---|---|
Enthalten in: |
Acta pharmaceutica Sinica. B - 14(2024), 1 vom: 23. Jan., Seite 350-364 |
Sprache: |
Englisch |
---|
Beteiligte Personen: |
Zhang, Yongshun [VerfasserIn] |
---|
Links: |
---|
Themen: |
Adeno-associated virus |
---|
Anmerkungen: |
Date Revised 25.01.2024 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
---|
doi: |
10.1016/j.apsb.2023.06.006 |
---|
funding: |
|
---|---|
Förderinstitution / Projekttitel: |
|
PPN (Katalog-ID): |
NLM36752256X |
---|
LEADER | 01000caa a22002652 4500 | ||
---|---|---|---|
001 | NLM36752256X | ||
003 | DE-627 | ||
005 | 20240125232123.0 | ||
007 | cr uuu---uuuuu | ||
008 | 240124s2024 xx |||||o 00| ||eng c | ||
024 | 7 | |a 10.1016/j.apsb.2023.06.006 |2 doi | |
028 | 5 | 2 | |a pubmed24n1270.xml |
035 | |a (DE-627)NLM36752256X | ||
035 | |a (NLM)38261817 | ||
040 | |a DE-627 |b ger |c DE-627 |e rakwb | ||
041 | |a eng | ||
100 | 1 | |a Zhang, Yongshun |e verfasserin |4 aut | |
245 | 1 | 0 | |a Combination of AAV-delivered tumor suppressor PTEN with anti-PD-1 loaded depot gel for enhanced antitumor immunity |
264 | 1 | |c 2024 | |
336 | |a Text |b txt |2 rdacontent | ||
337 | |a ƒaComputermedien |b c |2 rdamedia | ||
338 | |a ƒa Online-Ressource |b cr |2 rdacarrier | ||
500 | |a Date Revised 25.01.2024 | ||
500 | |a published: Print-Electronic | ||
500 | |a Citation Status PubMed-not-MEDLINE | ||
520 | |a © 2024 The Authors. | ||
520 | |a Recent clinical studies have shown that mutation of phosphatase and tensin homolog deleted on chromosome 10 (PTEN) gene in cancer cells may be associated with immunosuppressive tumor microenvironment (TME) and poor response to immune checkpoint blockade (ICB) therapy. Therefore, efficiently restoring PTEN gene expression in cancer cells is critical to improving the responding rate to ICB therapy. Here, we screened an adeno-associated virus (AAV) capsid for efficient PTEN gene delivery into B16F10 tumor cells. We demonstrated that intratumorally injected AAV6-PTEN successfully restored the tumor cell PTEN gene expression and effectively inhibited tumor progression by inducing tumor cell immunogenic cell death (ICD) and increasing immune cell infiltration. Moreover, we developed an anti-PD-1 loaded phospholipid-based phase separation gel (PPSG), which formed an in situ depot and sustainably release anti-PD-1 drugs within 42 days in vivo. In order to effectively inhibit the recurrence of melanoma, we further applied a triple therapy based on AAV6-PTEN, PPSGanti-PD-1 and CpG, and showed that this triple therapy strategy enhanced the synergistic antitumor immune effect and also induced robust immune memory, which completely rejected tumor recurrence. We anticipate that this triple therapy could be used as a new tumor combination therapy with stronger immune activation capacity and tumor inhibition efficacy | ||
650 | 4 | |a Journal Article | |
650 | 4 | |a Adeno-associated virus | |
650 | 4 | |a Antitumor immune response | |
650 | 4 | |a CpG | |
650 | 4 | |a Immune memory | |
650 | 4 | |a Immunogenic cell death | |
650 | 4 | |a PPSG@anti-PD-1 | |
650 | 4 | |a PTEN | |
650 | 4 | |a Triple therapy | |
700 | 1 | |a Yang, Lan |e verfasserin |4 aut | |
700 | 1 | |a Ou, Yangsen |e verfasserin |4 aut | |
700 | 1 | |a Hu, Rui |e verfasserin |4 aut | |
700 | 1 | |a Du, Guangsheng |e verfasserin |4 aut | |
700 | 1 | |a Luo, Shuang |e verfasserin |4 aut | |
700 | 1 | |a Wu, Fuhua |e verfasserin |4 aut | |
700 | 1 | |a Wang, Hairui |e verfasserin |4 aut | |
700 | 1 | |a Xie, Zhiqiang |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Yu |e verfasserin |4 aut | |
700 | 1 | |a He, Chunting |e verfasserin |4 aut | |
700 | 1 | |a Ma, Cheng |e verfasserin |4 aut | |
700 | 1 | |a Gong, Tao |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Ling |e verfasserin |4 aut | |
700 | 1 | |a Zhang, Zhirong |e verfasserin |4 aut | |
700 | 1 | |a Sun, Xun |e verfasserin |4 aut | |
773 | 0 | 8 | |i Enthalten in |t Acta pharmaceutica Sinica. B |d 2012 |g 14(2024), 1 vom: 23. Jan., Seite 350-364 |w (DE-627)NLM227628217 |x 2211-3835 |7 nnns |
773 | 1 | 8 | |g volume:14 |g year:2024 |g number:1 |g day:23 |g month:01 |g pages:350-364 |
856 | 4 | 0 | |u http://dx.doi.org/10.1016/j.apsb.2023.06.006 |3 Volltext |
912 | |a GBV_USEFLAG_A | ||
912 | |a GBV_NLM | ||
951 | |a AR | ||
952 | |d 14 |j 2024 |e 1 |b 23 |c 01 |h 350-364 |