Molecular Vision 2011; 17:1694-1700
Received 28 April 2011 | Accepted 21 June 2011 | Published 25 June 2011
The first two authors contributed equally to this work
1State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Guangzhou, China; 2Department of Ophthalmology, The Third Affiliated Hospital of Sun Yat-sen University, Guangzhou, China
Correspondence to: Haotian Lin, State Key Laboratory of Ophthalmology, Zhongshan Ophthalmic Center, Sun Yat-sen University, Xian Lie Nan Road 54#, Guangzhou, China 510060; Phone: +86013802793086; FAX: +86-20-87333271; email: email@example.com
Purpose: To investigate the relationship of (lymph) angiogenesis and survival time of human cornea grafts.
Methods: This was a case series study. A total of 250 patients requiring a second keratoplasty were screened according to our inclusion criteria: 1) only cases with primary non-inflamed cornea diseases were included; and 2) all primary diseased cornea specimens from the first corneal transplantation were confirmed not to have hemangiogenesis or lymphangiogenesis. The included patients were analyzed retrospectively and followed up for the survival time of the first and second grafts. Blood vessel content (BVC) and lymphatic vessel content (LVC) were assessed in the primary diseased cornea; first rejected grafts (including BVC1 and LVC1) and second rejected grafts (including BVC2 and LVC2) were assessed by immunohistochemistry. The survival times of the first (STG1) and second (STG2) rejected corneal grafts were calculated and the relationship between human corneal (lymph) angiogenesis and STG was statistically analyzed.
Results: After screening, only 23 patients (23 eyes) were included. Their primary cornea diseases were non-inflamed, including keratoconus (n=14), leukoma (n=5), and Fuchs endothelial dystrophy (n=4). The mean duration of follow up was 36 months after the second keratoplasty. In all, 55 cornea specimens from different times following penetrating keratoplasty were collected and examined, including 23 primary non-inflamed corneas (without angiogenesis), 23 first rejected corneal grafts (all with hemangiogenesis, but only six cases with blown lymphatic vessels), and nine rejected corneal grafts (including six cases identified with lymphangiogenesis in the first rejection, all with lymphangiogenesis and hemangiogenesis). Based on our statistical analysis, STG1 was correlated with LVC1 but not with BVC1 or (LVC1+BVC1), while STG2 was correlated with (LVC1+LVC2), LVC1, LVC2, (LVC2+BVC2) and (LVC1+BVC1) but not with BVC1 or BVC2.
Conclusions: The survival time of human cornea grafts is related to both lymphangiogenesis and hemangiogenesis. Lymphangiogenesis only occurred in some rejected cases, but it seems to be a signal of poor prognosis for the new allograft.
The major cause of corneal allograft failure is considered to be immunological rejection [1-5], which depends on both hemangiogenesis and lymphangiogenesis. These co-occur as two arms of an immune reflex arc and accelerate immune reactions leading to corneal rejection [6-8]. Numerous studies have been conducted on the processes of corneal blood vessel proliferation, whereas reports on corneal lymphangiogenesis are relatively scarce, especially for transplanted human corneas [8,9]. We previously reported that lymphangiogenesis occurred after corneal transplantation in both rats and humans . However, without detailed clinical data, the relationship of angiogenesis and graft survival time cannot be determined, nor can the system (lymphatic system or blood vessels) that plays the most important role in accelerating graft rejections [5,11,12] be determined. In the present research, we began our clinical study by screening out cases of hospitalized patients who had previously received penetrating keratoplasty because of non-inflamed corneal diseases (taken to mean no hemangiogenesis or lymphangiogenesis) , but now have experienced corneal graft rejection and require a second keratoplasty. All of the included patients were followed up until the second corneal allograft failed and needed a third transplantation or ophthalmectomy. Each cornea specimen was assessed for blood vessel content (BVC) and lymphatic vessel content (LVC) by immunohistochemistry with antibodies specific for CD31 (vWF) and the lymphatic endothelial markers (lymphatic vessel endothelial hyaluronan receptor [LYVE-1]). The survival time of the graft (STG) was recorded and statistically analyzed together with the pathology results.
In total, 250 hospitalized patients, who required a second keratoplasty because of graft failure occurring during January 2005 to December 2008, were screened. Only patients who met the inclusion criteria were included in our study. The protocol and informed consent forms were reviewed and approved by the Institutional Review Board/Ethics Committee of Sun Yat-sen University and a written informed consent form was completed by each study participant. The study was conducted in accordance with the Declaration of Helsinki and the ethical standards of the local ethics committee.
Primary diseases for the first keratoplasty were non-inflamed cornea diseases. No systemic immune diseases were found and no immunosuppressant was used preoperatively. All of the original diseased cornea specimens (obtained from the first corneal transplantation) from the included patients were confirmed to be without hemangiogenesis and lymphangiogenesis by immunohistochemistry [6,14] and all cornea specimens were identified to be vWF-/LYVE-1-(Detailed methods are described below). All of the patients received second or third penetrating keratoplasty within one week after identification of signs of graft rejection (The time interval between the first and second, or second and third penetrating keratoplasty could be considered as the survival time of the first or second corneal allograft.). All of the diseased/rejected corneas were available and were collected, and all of the included patients provided signed consent and could be followed up according to our schedule.
Penetrating keratoplasty was performed on all included patients according to standard methods  and they received the same immunosuppressive agents after each keratoplasty. The detailed regimen included:
1: 0.5% Tacrolimus Eye Drops, Qid for three months;
2: Compound Tobramycin Eye Drops: 0.3% tobramycin + 0.1% dexamethasone, Qid for one month;
3: Oral Predinisone 1mg/(kg/d), Qid, tapering by 20% every week, use for four weeks.
After the second keratoplasty, patients were followed up every four weeks (one month) until the second corneal allograft failed and they required a third transplantation or ophthalmectomy.
After corneas were sent to our Ocular Pathology Laboratory for histopathologic evaluation, they were fixed in 10% neutral formalin for 24 h, embedded in paraffin and sectioned (4 μm sections: 20 sections were from the central part of each cornea and the other 20 slices were from peripheral part). All sections of rejected corneas were rehydrated with graded ethanol-water mixtures, washed with distilled water, and then endogenous peroxidase activity was blocked by incubation with 30 ml/l hydrogen peroxidase for 20 min. Every two neighboring sections were selected and stained with streptavidin-biotin complex. The chosen cornea sections were incubated for 3 h with mouse anti-human LYVE-1 polyclonal antibody (R&D Systems, Minneapolis, MN) and mouse anti-human cluster of differentiation 31 (CD31; R&D Systems). The slices were incubated with biotin-marked rabbit anti-mouse immunoglobulin (Boster, Wuhan, China) as the secondary antibody. Finally, after incubation with streptavidin-biotin horseradish peroxidase (SAB-HRP) complex (Boster) at room temperature for 30 min, the slides were visualized for peroxidase activity with diaminobenzidine and counterstained with hematoxylin.
Lymphatic vessel content (LVC) and blood vessel content (BVC) of the human corneas were evaluated independently by two observers who had no prior knowledge of the experimental details, and the evaluations were repeated twice. The CD31(+) LYVE-1(-) stained vessels in cornea slices were identified as blood vessels, whereas the CD31(+) LYVE-1(+) vessels were identified as lymphatic vessels. Each cornea sample was sliced into 40 slices (20 slices were from central part and the other 20 slices were from peripheral part of each cornea). The BVC was calculated by summing all blood vessels in the 40 slices and dividing by 40. Similarly, LVC was calculated by summing all lymphatic vessels in the 40 slices and dividing by 40 [6,8,14].
Analysis of the significance of difference was performed using the paired Student’s t test for normally distributed data (BVC1, LVC1+BVC1 and STG1) and ANOVA for non-normally distributed data (STG2, BVC2, LVC1, LVC2, LVC2+BVC2; with the use of SPSS software [version 17.0; SPSS, Inc., Chicago, IL]). A multivariate model for STG was developed. Values are presented as mean±SD. Differences were accepted as significant when p<0.05.
Screening of 250 patients with corneal graft rejection identified only 23 patients (23 eyes, 15 male and 8 female; mean age, 50±14 years; range, 18–69) for inclusion in the study. Primary non-inflamed cornea diseases included keratoconus (n=14), leukoma (n=5), and Fuchs endothelial dystrophy (n=4). After the second keratoplasty, patients were followed up every month. The mean duration of follow up was three years (average 36 months, 26–42 months) after the second keratoplasty. In nine cases, the second transplanted corneas were rejected during our follow up. (In these 9 cases of second rejection, 4 patients received a third corneal transplantation, but the other 5 patients had to undergo ophthalmectomy for lack of any better choice.) The other 14 cases of second transplanted corneas are still functioning. In all, 55 cornea specimens from penetrating keratoplasty or ophthalmectomy, including 23 non-vascularized corneas (primary non-inflamed diseases), 23 first rejected corneal grafts, and nine rejected corneal grafts, were obtained for examination in this study.
According to our designation, the survival time of the first corneal allograft (STG1) was estimated as the time interval between the first and second penetrating keratoplasty (23 eyes, 18.478±7.089 months; range, 3–33 months). In these 23 rejected allografts, 17 cases presented mild hemangiogenesis (Figure 1A), but the other six cases presented severe hemangiogenesis and inflammation (Figure 1B), as determined by slit lamp examination. The survival time of the second corneal graft (STG2) was calculated as the time interval between the second and third penetrating keratoplasty or ophthalmectomy (nine eyes were rejected, 9.000±5.477months; range, 2–17 months; the other 14 cases are still functioning). In these second rejected cases, four patients received a third corneal transplantation (Figure 1C), but the other five patients had to receive ophthalmectomy (Figure 1D) for lack of a better choice.
The first antibody for CD31 for immunohistochemistry revealed a positive (brown) staining for CD31 in lymphatic vessels and blood vessels (brown), as shown in Figure 2A. The first antibody for LYVE-1 in a neighboring cornea slice showed positive (brown) stain for lymphatic vessels but blood vessels were negative (no staining) for LYVE-1, as shown in Figure 2B. The brown corneal lymphangiogenesis appeared like vessels or strips, along with blue vessels that were scattered within the positive stroma [6,8,10,14]. From the first corneal transplantation, none of the primary cornea specimens with original diseases showed hemangiogenesis or lymphangiogenesis. From the second corneal transplantation, we found that 17 cases of the first rejected cornea that presented with mild hemangiogenesis by slip lamp examination (Figure 1A), which was confirmed by immunohistochemistry that showed hemangiogenesis occurring and inflammation cells infiltrating. However, the other 6 cases of first rejected corneas (Figure 1B) showed both hemangiogenesis and lymphangiogenesis. All nine cases (Figure 1C,D) of second rejected transplanted cornea were confirmed to show hemangiogenesis and lymphangiogenesis.
The relationships of STG, hemangiogenesis, and lymphangiogenesis at different times of corneal transplantation are shown in Figure 3.
The clinical data of STG1 and STG2 and the pathological results of immunochemistry for LVC and BVC allowed us to perform statistical analysis of the relationship of angiogenesis and graft survival time and to determine which one (lymphatic or blood vessels) may play the most important role in promoting corneal graft rejections. The paired Student t test was used to compare the correlation between STG and LVC, BVC or both (Table 1). The STG1 showed a significant correlation with LVC1 (Correlation=-0.577, p=0.004) but not with BVC1 or (LVC1+BVC1); STG2 has a significant correlation with (LVC1+LVC2), LVC1, LVC2, (LVC2+BVC2) and (LVC1+BVC1) (all with p<0.05, and the correlation coefficients were all negative, with values from largest to smallest.) but not with BVC1 or BVC2 (p>0.05). Based on our statistical analysis, we could see that the survival time of human cornea grafts (STG) was related both with lymphangiogenesis (LVC) and hemangiogenesis (BVC), but lymphangiogenesis (LVC) may play a more important role.
A normal-risk keratoplasty usually has a successful outcome and this is attributed to corneal immune privilege . The lack of both afferent lymphatic and efferent blood vessels in the cornea prevents operation of either arm of an immune reflex arc and is the most important cause of privilege among all factors [11,12,15,16]. For a high-risk keratoplasty, preexisting corneal stromal blood vessels have been identified as a strong risk factor for immune rejection after corneal transplantation, both in the clinical setting and in the well-defined mouse model of corneal transplantation [11,15,17]. Recently, in addition to blood vessels (the efferent arm of an immune reflex arc: access for immune effectors cells to the graft), lymphatic vessels that are microscopically undetectable have been found in association with blood vessels in vascularized high-risk human corneas . These lymphatic vessels enable effective access of donor and host antigen-presenting cells (APCs) and antigenic material to regional lymph nodes, where accelerated sensitization to graft antigens occurs (the afferent arm of an immune reflex arc) [5-8,18]. Yamagami et al.  have successfully inhibited allograft rejection of mice after obstruction of corneal lymph drainage by bilateral cervical lymphadenectomy [20,21]. Their later study showed that the survival rate of corneal grafts placed into vascularized recipient beds was as high as 92%21, which suggested that lymphangiogenesis plays a more important role in allograft rejection than does corneal hemangiogenesis in animal models.
Research into human corneal lymphangiogenesis has been scarce until now. Claus Cursiefen first reported that lymphatic vessels existed in vascularized human corneas . In his report, lymphatic vessels were found in 10 out of 21 cases of vascularized human corneas caused by different diseases. In our previous study , we also reported that lymphangiogenesis occurred in mouse and human transplanted corneas, but the clinical role of lymphangiogenesis in allograft rejection (accelerating or preventing rejection) still awaited identification [5,21]. Many immunology related questions are still unanswered, such as: whether preexisting corneal stromal blood vessels are an essential condition for the lymphangiogenesis process; whether lymphangiogenesis implies inevitable corneal graft rejection; the nature of the relationship of angiogenesis and graft survival time; and which (lymphatic or blood vessels) may play a more important role in accelerating corneal graft rejections. The present study was designed to answer these questions by clinicopathological analysis of angiogenesis and corneal graft rejection.
According to our inclusion criteria, only cases with primary non-inflamed cornea diseases were included. All of the primary diseased cornea specimens from the first corneal transplantation were confirmed to show no hemangiogenesis or lymphangiogenesis. Therefore, the first corneal transplantation could be considered as a normal-risk keratoplasty and preexisting corneal stromal (lymph) angiogenesis is apparently not an essential condition for allograft rejection. However, for the second corneal transplantation, we found that 17 cases of rejected allografts were confirmed with only hemangiogenesis occurring and with immunochemistry showing infiltration with inflammation cells, while six cases of rejected corneas showed both hemangiogenesis and lymphangiogenesis processes. The positive rate of lymphangiogenesis was 26.1%, which is much lower than the value reported in vascularized human corneas (48%) by Cursiefen et al. . Two reasons may explain this: First, all patients received a second penetrating keratoplasty within one week of identifying the sign of the graft rejection, so the time may be not have been long enough for development of lymphangiogenesis. Second, the primary cornea diseases of all the cases in our study were non-inflammatory, without hemangiogenesis or lymphangiogenesis. Lymphangiogenesis may be induced by or lead to allograft rejection, which should be further confirmed in the future study. Based on the third surgery, all nine cases of second rejected allograft were confirmed with hemangiogenesis and lymphangiogenesis. In these nine cases, six cases had been identified with preexisting corneal stromal hemangiogenesis or lymphangiogenesis from the second cornea transplantation, and the STG2 is obviously shorter than the other allograft. Lymphangiogenesis only occurred in some rejected cases, but it seems to be a signal of poor prognosis for the new allograft.
We investigated the relationship of lymphangiogenesis and corneal graft rejections further by statistical analysis of the correlation of STG, LVC, and BVC of different corneal allografts. We found that both hemangiogenesis and lymphangiogenesis were significantly correlated with STG. The second corneal grafts, in particular, when placed into lymphatic-vascularized recipient beds, would fail quickly with additional and more severe lymphangiogenesis and hemangiogenesis. In other words, similar to the implication of lymphangiogenesis for tumor metastasis [13,22-24], new allograft rejection is predictable and inevitable when lymphangiogenesis is found in corneal recipient beds [11,25].
In conclusion, the survival time of a human cornea graft is associated with both lymphangiogenesis and hemangiogenesis, and lymphangiogenesis is a signal of poor prognosis for the new allograft.
We thank Huang Li for help in statistical analysis of our data in the paper. The authors declare that they have no competing interests. Supported by the National Natural Science Foundation of China (81000389), Guangdong Natural Science Foundation (10451008901004945), Guangdong Provincial Science and Technology program (2008B060600026 and 2009B060700089), Youth Projects of Medical Research Fund of Guangdong Province (B2010107), and Fundamental Research Funds of State Key Laboratory of Ophthalmology.