TY - JOUR
T1 - Cancer immune therapy for lymphoid malignancies
T2 - recent advances
AU - Klausen, Uffe
AU - Jørgensen, Nicolai Grønne Dahlager
AU - Grauslund, Jacob Handlos
AU - Holmström, Morten Orebo
AU - Andersen, Mads Hald
PY - 2019/1
Y1 - 2019/1
N2 - Immunotherapy has played an important part in improving the life of patients with lymphoproliferative diseases especially since the addition of rituximab to chemotherapy in the CD20-positive neoplasms in the 1990s. While this field of passive immunotherapy is continuously evolving, several breakthroughs will expand the treatment modalities to include more active immunotherapy. With the approval of immune checkpoint-blocking antibodies for Hodgkin lymphoma and bispecific antibodies for acute lymphoblastic leukemia (ALL), activation of endogenous T cells already plays a role in several lymphoid malignancies. With the approval of cellular therapies with CAR-T cells for ALL and diffuse large B cell lymphoma, the impact of the manipulation of immune responses is taken even further. Vaccines are cellular therapies in the opposite end of the spectrum in terms of side effects, and while the big breakthrough is still to come, the prospect of a very low-toxic immunotherapy which could be applicable also in premalignant states or in frail patients drives a considerable research activity in the area. In this review, we summarize the mechanisms of action and clinical data on trials in the lymphoid neoplasms with chimeric antigen receptor T cells, bispecific antibodies, immune checkpoint-blocking antibodies, and antineoplastic vaccination therapy.
AB - Immunotherapy has played an important part in improving the life of patients with lymphoproliferative diseases especially since the addition of rituximab to chemotherapy in the CD20-positive neoplasms in the 1990s. While this field of passive immunotherapy is continuously evolving, several breakthroughs will expand the treatment modalities to include more active immunotherapy. With the approval of immune checkpoint-blocking antibodies for Hodgkin lymphoma and bispecific antibodies for acute lymphoblastic leukemia (ALL), activation of endogenous T cells already plays a role in several lymphoid malignancies. With the approval of cellular therapies with CAR-T cells for ALL and diffuse large B cell lymphoma, the impact of the manipulation of immune responses is taken even further. Vaccines are cellular therapies in the opposite end of the spectrum in terms of side effects, and while the big breakthrough is still to come, the prospect of a very low-toxic immunotherapy which could be applicable also in premalignant states or in frail patients drives a considerable research activity in the area. In this review, we summarize the mechanisms of action and clinical data on trials in the lymphoid neoplasms with chimeric antigen receptor T cells, bispecific antibodies, immune checkpoint-blocking antibodies, and antineoplastic vaccination therapy.
KW - Animals
KW - Antibodies, Bispecific/pharmacology
KW - Antineoplastic Agents, Immunological/therapeutic use
KW - Biomarkers, Tumor
KW - Cancer Vaccines
KW - Humans
KW - Immunotherapy/methods
KW - Immunotherapy, Adoptive/methods
KW - Leukemia, Lymphoid/diagnosis
KW - Lymphoma/diagnosis
KW - Receptors, Chimeric Antigen/genetics
KW - T-Lymphocyte Subsets/immunology
KW - Vaccination
U2 - 10.1007/s00281-018-0696-7
DO - 10.1007/s00281-018-0696-7
M3 - Review
C2 - 30006739
SN - 1863-2297
VL - 41
SP - 111
EP - 124
JO - Seminars in Immunopathology
JF - Seminars in Immunopathology
IS - 1
ER -