TY - JOUR
T1 - Mechanisms of blood-retinal barrier disruption related to intraocular inflammation and malignancy
AU - Tomkins-Netzer, Oren
AU - Niederer, Rachael
AU - Greenwood, John
AU - Fabian, Ido Didi
AU - Serlin, Yonatan
AU - Friedman, Alon
AU - Lightman, Sue
N1 - Publisher Copyright:
© 2024
PY - 2024/3/1
Y1 - 2024/3/1
N2 - Blood-retinal barrier (BRB) disruption is a common accompaniment of intermediate, posterior and panuveitis causing leakage into the retina and macular oedema resulting in vision loss. It is much less common in anterior uveitis or in patients with intraocular lymphoma who may have marked signs of intraocular inflammation. New drugs used for chemotherapy (cytarabine, immune checkpoint inhibitors, BRAF inhibitors, EGFR inhibitors, bispecific anti-EGFR inhibitors, MET receptor inhibitors and Bruton tyrosine kinase inhibitors) can also cause different types of uveitis and BRB disruption. As malignant disease itself can cause uveitis, particularly from breast, lung and gastrointestinal tract cancers, it can be clinically difficult to sort out the cause of BRB disruption. Immunosuppression due to malignant disease and/or chemotherapy can lead to infection which can also cause BRB disruption and intraocular infection. In this paper we address the pathophysiology of BRB disruption related to intraocular inflammation and malignancy, methods for estimating the extent and effect of the disruption and examine why some types of intraocular inflammation and malignancy cause BRB disruption and others do not. Understanding this may help sort and manage these patients, as well as devise future therapeutic approaches.
AB - Blood-retinal barrier (BRB) disruption is a common accompaniment of intermediate, posterior and panuveitis causing leakage into the retina and macular oedema resulting in vision loss. It is much less common in anterior uveitis or in patients with intraocular lymphoma who may have marked signs of intraocular inflammation. New drugs used for chemotherapy (cytarabine, immune checkpoint inhibitors, BRAF inhibitors, EGFR inhibitors, bispecific anti-EGFR inhibitors, MET receptor inhibitors and Bruton tyrosine kinase inhibitors) can also cause different types of uveitis and BRB disruption. As malignant disease itself can cause uveitis, particularly from breast, lung and gastrointestinal tract cancers, it can be clinically difficult to sort out the cause of BRB disruption. Immunosuppression due to malignant disease and/or chemotherapy can lead to infection which can also cause BRB disruption and intraocular infection. In this paper we address the pathophysiology of BRB disruption related to intraocular inflammation and malignancy, methods for estimating the extent and effect of the disruption and examine why some types of intraocular inflammation and malignancy cause BRB disruption and others do not. Understanding this may help sort and manage these patients, as well as devise future therapeutic approaches.
KW - Blood-retinal barrier
KW - Cytokines
KW - Fluorescein angiography
KW - Lymphoma
KW - Uveitis
KW - Vascular endothelial growth factor
UR - http://www.scopus.com/inward/record.url?scp=85185151514&partnerID=8YFLogxK
U2 - 10.1016/j.preteyeres.2024.101245
DO - 10.1016/j.preteyeres.2024.101245
M3 - Review article
C2 - 38242492
AN - SCOPUS:85185151514
SN - 1350-9462
VL - 99
JO - Progress in Retinal and Eye Research
JF - Progress in Retinal and Eye Research
M1 - 101245
ER -