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1 les in these mice induced acute rejection of corneal grafts.
2 nition have the ability to reject allogeneic corneal grafts.
3 ents for orthotopic syngeneic and allogeneic corneal grafts.
4 ulceration, or corneal neovascularization on corneal grafts.
5 Of the DMEKs, 196 (55%) used preloaded corneal grafts.
6 estigated whether CHIKV is transmittable via corneal grafts.
7 onors of combined MHC and minor H-mismatched corneal grafts.
8 ecessary for the rejection of MHC-mismatched corneal grafts.
9 o play in determining the fate of orthotopic corneal grafts.
10 gene expression in syngeneic and allogeneic corneal grafts.
11 ossed corneal surface wounds, and orthotopic corneal grafting.
13 (11.8% vs 0%, P = .03), previous history of corneal graft (20.6% vs 0%, P = .0012), and prior topica
15 e hydrops, and have improved the survival of corneal grafts after transplantation for resolved hydrop
16 likely to perforate or require an emergency corneal graft, after adjusting for baseline ulcer depth
17 eal grafts had swift rejection of subsequent corneal grafts and exhibited strong donor-specific DTH.
18 ity, intraocular pressure (IOP), survival of corneal grafts, and success of glaucoma surgery (defined
21 presenting passenger Langerhans cells in the corneal graft; (b) expression of Fas ligand on the epith
24 o receive a B-KPro using a frozen or a fresh corneal graft carrier on the basis of tissue availabilit
25 erm clinical outcomes of fresh versus frozen corneal graft carriers for the Boston Keratoprosthesis t
28 significantly increased opacity of C57BL/6J corneal grafts, compared with the relatively clear graft
29 low-risk eyes of mice, most of the composite corneal grafts composed of syngeneic epithelium layered
31 at at least three additional features of the corneal graft contribute to its immune privileged status
32 elial keratoplasty cases that used preloaded corneal grafts cost $460.19 less ($316.23-$604.14; P < 0
33 mph nodes (LNs), we tracked the migration of corneal graft-derived transgenic green fluorescent prote
34 is promotes systemic Th2 immune responses to corneal graft donor alloantigens; 2) corneal allografts
35 iver exogenous gene(s) to the endothelium of corneal grafts during hypothermic organ preservation.
36 ons included retinal detachment (2), chronic corneal graft failure (2), phthisis (1) and band keratop
37 The most common indication for surgery was corneal graft failure (n = 50; 44%) followed by chemical
38 PKP has significant implications leading to corneal graft failure and irreversible vision loss from
41 favorable outcomes of KPro surgery for donor corneal graft failure with a greater likelihood of maint
42 electronic medical records and evaluated for corneal graft failure, defined as irreversible and visua
46 of MHC-matched, multiple minor H-mismatched corneal grafts fell from 80% in untreated controls to 36
51 - and wild-type C57BL/6 (ICAM-1+/+) received corneal grafts from the following strains of mice: BALB/
52 nstituted with CLNs from hosts with rejected corneal grafts had swift rejection of subsequent corneal
55 s results in the permanent acceptance of NZB corneal grafts in 60% and 90% of the CB6F1 hosts, respec
56 orneal grafts showed rejection of subsequent corneal grafts in a manner that was indistinguishable fr
59 rence in survival of fully-mismatched BALB/c corneal grafts in p55-/- (n=12; P=0.76) or in double-kno
60 rvival of minor alloantigen-disparate BALB.b corneal grafts in p75-/- (n=13; P=0.95) or in combined p
61 There were more perforations and emergency corneal grafts in the chlorhexidine arm (24/175, 13.7%)
63 ophthalmologic examination before and after corneal graft, including VA, assessed by the preferentia
66 To examine the widely accepted dogmas that corneal grafts lack passenger leukocytes or cells capabl
70 on were activated directly in both skin- and corneal-grafted mice, only CD8+ T cells from skin-transp
71 unized hosts rejected their fully allogeneic corneal grafts (MST = 43 days) compared with 100% reject
76 These studies have been extended to include corneal grafts placed in neovascularized high-risk eyes
78 ce who had already been primed by a previous corneal graft, prevented rejection of a second corneal g
80 ng sixty eyes (60 patients) at high risk for corneal graft rejection (GR) because of previous immunol
81 les, saline, or DSP in solution demonstrated corneal graft rejection accompanied by severe corneal ed
82 ickness (En/DMT) are of predictive value for corneal graft rejection after high-risk corneal transpla
83 ncompatibility (including H-Y mismatches) on corneal graft rejection and failure was evaluated using
84 that CD8(+) CTLs are essential in promoting corneal graft rejection and instead further implicates d
85 tion of allospecific effector macrophages in corneal graft rejection and the role of CD4(+) T cells a
86 y selected controls who did not experience a corneal graft rejection at their matched cases' index da
87 icroscopy (IVCM) can aid in the diagnosis of corneal graft rejection by detecting cellular corneal ch
90 tained release of corticosteroids to prevent corneal graft rejection following subconjunctival inject
91 unct to prevent graft neovascularization and corneal graft rejection in high-risk corneal transplants
94 Thus, MHC matching may reduce the risk of corneal graft rejection in patients with atopic keratoco
95 study is to develop a pre-clinical model of corneal graft rejection in the semi-inbred NIH minipig a
97 eye, so the required frequency of dosing for corneal graft rejection management can be as high as onc
98 rts have documented uveitis flares and acute corneal graft rejection occurring within the first 3 wee
100 HC matching dramatically reduces the risk of corneal graft rejection when IFN-gamma is depressed or a
101 ., the SM node, is the major DLN involved in corneal graft rejection whereas its nearest neighbor, th
103 approach for safely preventing and treating corneal graft rejection with the potential for improved
104 with penetrating keratoplasty (15 eyes with corneal graft rejection, 23 eyes without rejection) and
105 uggested a role for Fas-induced apoptosis in corneal graft rejection, additional experiments indicate
106 Alloantibody, although not necessary for corneal graft rejection, can produce extensive injury to
107 se of corticosteroids may reduce the rate of corneal graft rejection, perhaps especially in the days
126 nstituted with CLNs from hosts with accepted corneal grafts showed rejection of subsequent corneal gr
128 ic epithelium protects orthotopic allogeneic corneal grafts (stroma plus endothelium) placed in high-
131 BAT glare responses identified that the hazy corneal graft surrounding the KPro is the main source of
132 i-CD80/86 antibodies significantly prolonged corneal graft survival and decreased IFN-gamma(+)-produc
133 cells is an effective strategy for enhancing corneal graft survival and preventing graft rejection in
134 uded change in best corrected visual acuity, corneal graft survival and retinal reattachment at final
135 specific immune tolerance leads to long-term corneal graft survival as evidenced by the higher surviv
136 i-CD80/86 antibodies significantly prolonged corneal graft survival by inhibiting T-cell proliferatio
137 tion can successfully restore sight in many, corneal graft survival decreases in eyes with chronic in
139 munization with donor corneal cells enhanced corneal graft survival in all three high-risk settings.
140 Results showed a significant increase in corneal graft survival in alpha-MSH-treated recipients c
143 c cells to induce oral tolerance and enhance corneal graft survival indicates that oral tolerance to
147 B), was examined for its capacity to enhance corneal graft survival when given separately or conjugat
148 t with normal hamster serum had no effect on corneal graft survival, infusion of anti-gamma delta Ab
149 fixed cells retain their capacity to enhance corneal graft survival, it may be possible to store dono
153 h a TKP are performed, approximately half of corneal grafts survive, anatomically successful retinal
156 Rag(-/-) mice, both allogeneic and syngeneic corneal grafts survived; endostatin remained high throug
157 as covered by a 300-micron partial thickness corneal graft taken either from a previous Descemet stri
159 ing induction vs effector of alloimmunity in corneal grafts, the most common form of tissue transplan
160 In addition, a global shortage of cadaveric corneal graft tissue critically limits accessibility to
161 ally quantified the considerable shortage of corneal graft tissue, with only 1 cornea available for 7
162 the long-term outcomes of partial thickness corneal grafts to cover the tube and prevent its exposur
163 fore and after surgery, mean follow-up time, corneal graft type, long-term complications, need for ad
168 gamma-producing CD4(+) T cell frequencies in corneal grafts were assessed with intraperitoneal inject
174 he posterior surface of accepted or rejected corneal grafts, whereas bone marrow-derived cells of rec
175 ss than 10% of the uncomplicated, first-time corneal grafts will undergo immune rejection even though
176 st deficiency in ICAM-1 promotes survival of corneal grafts with different degrees of allodisparity.