A new era of macrophage-based cell therapy

被引:66
作者
Na, Yi Rang [1 ]
Kim, Sang Wha [2 ,3 ]
Seok, Seung Hyeok [2 ,3 ,4 ,5 ,6 ]
机构
[1] Seoul Natl Univ Hosp, Dept Transdisciplinary Med, Translat Immunol Lab, Seoul, South Korea
[2] Seoul Natl Univ, Coll Med, Dept Microbiol & Immunol, Macrophage Lab, Seoul 110799, South Korea
[3] Seoul Natl Univ, Coll Med, Inst Endem Dis, Seoul 110799, South Korea
[4] Seoul Natl Univ, Dept Biomed Sci, Seoul, South Korea
[5] Seoul Natl Univ, Dept Biomed Sci, Coll Med, Seoul, South Korea
[6] Seoul Natl Univ, Coll Med, Canc Res Inst, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
BLOOD MONOCYTES; TRANSPLANTATION; IMMUNOTHERAPY; SAFETY; LONG;
D O I
10.1038/s12276-023-01068-z
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Macrophages are essential innate immune cells found throughout the body that have protective and pathogenic functions in many diseases. When activated, macrophages can mediate the phagocytosis of dangerous cells or materials and participate in effective tissue regeneration by providing growth factors and anti-inflammatory molecules. Ex vivo-generated macrophages have thus been used in clinical trials as cell-based therapies, and based on their intrinsic characteristics, they outperformed stem cells within specific target diseases. In addition to the old methods of generating naive or M2 primed macrophages, the recently developed chimeric antigen receptor-macrophages revealed the potential of genetically engineered macrophages for cell therapy. Here, we review the current developmental status of macrophage-based cell therapy. The findings of important clinical and preclinical trials are updated, and patent status is investigated. Additionally, we discuss the limitations and future directions of macrophage-based cell therapy, which will help broaden the potential utility and clinical applications of macrophages.
引用
收藏
页码:1945 / 1954
页数:10
相关论文
共 55 条
[1]  
ANDREESEN R, 1990, CANCER RES, V50, P7450
[2]   Adoptive immunotherapy of cancer using monocyte-derived macrophages: rationale, current status, and perspectives [J].
Andreesen, R ;
Hennemann, B ;
Krause, SW .
JOURNAL OF LEUKOCYTE BIOLOGY, 1998, 64 (04) :419-426
[3]   3 CLONAL TYPES OF KERATINOCYTE WITH DIFFERENT CAPACITIES FOR MULTIPLICATION [J].
BARRANDON, Y ;
GREEN, H .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (08) :2302-2306
[4]   Engineering the next generation of cell-based therapeutics [J].
Bashor, Caleb J. ;
Hilton, Isaac B. ;
Bandukwala, Hozefa ;
Smith, Devyn M. ;
Veiseh, Omid .
NATURE REVIEWS DRUG DISCOVERY, 2022, 21 (09) :655-675
[5]   Islet cell transplantation for the treatment of type 1 diabetes: recent advances and future challenges [J].
Bruni, Anthony ;
Gala-Lopez, Boris ;
Pepper, Andrew R. ;
Abualhassan, Nasser S. ;
Shapiro, A. M. James .
DIABETES METABOLIC SYNDROME AND OBESITY-TARGETS AND THERAPY, 2014, 7 :211-223
[6]   Extracellular Vesicle-Educated Macrophages Promote Early Achilles Tendon Healing [J].
Chamberlain, Connie S. ;
Clements, Anna E. B. ;
Kink, John A. ;
Choi, Ugeun ;
Baer, Geoffrey S. ;
Halanski, Matthew A. ;
Hematti, Peiman ;
Vanderby, Ray .
STEM CELLS, 2019, 37 (05) :652-662
[7]   Safety and Therapeutic Potential of M2 Macrophages in Stroke Treatment [J].
Chernykh, Elena R. ;
Shevela, Ekaterina Ya. ;
Starostina, Nataliya M. ;
Morozov, Sergey A. ;
Davydova, Mariya N. ;
Menyaeva, Elena V. ;
Ostanin, Alexandr A. .
CELL TRANSPLANTATION, 2016, 25 (08) :1461-1471
[8]   Adoptive transfer of immunomodulatory M2 macrophages suppresses experimental autoimmune encephalomyelitis in C57BL/6 mice via blockading NF-κB pathway [J].
Chu, F. ;
Shi, M. ;
Lang, Y. ;
Chao, Z. ;
Jin, T. ;
Cui, L. ;
Zhu, J. .
CLINICAL AND EXPERIMENTAL IMMUNOLOGY, 2021, 204 (02) :199-211
[9]   Lancet Commission: Stem cells and regenerative medicine [J].
Cossu, Giulio ;
Birchall, Martin ;
Brown, Tracey ;
De Coppi, Paolo ;
Culme-Seymour, Emily ;
Gibbon, Sahra ;
Hitchcock, Julian ;
Mason, Chris ;
Montgomery, Jonathan ;
Morris, Steve ;
Muntoni, Francesco ;
Napier, David ;
Owji, Nazanin ;
Prasad, Aarathi ;
Round, Jeff ;
Saprai, Prince ;
Stilgoe, Jack ;
Thrasher, Adrian ;
Wilson, James .
LANCET, 2018, 391 (10123) :883-910
[10]   Treatment of human ulcers by application of macrophages prepared from a blood unit [J].
Danon, D ;
Madjar, J ;
Edinov, E ;
Knyszynski, A ;
Brill, S ;
Diamantshtein, L ;
Shinar, E .
EXPERIMENTAL GERONTOLOGY, 1997, 32 (06) :633-641