Year : 2004 | Volume
: 52 | Issue : 1 | Page : 51--56
Elevated free tear lactoferrin levels in leprosy are associated with type 2 reactions
E Daniel, M Duriasamy, Gigi J Ebenezer, Shobhana, Charles K Job
Department of Ophthalmology, Schieffelin Leprosy Research and Training Center, Tamil Nadu, India
Department of Ophthalmology, Schieffelin Leprosy Research and Training Center, Tamil Nadu
Purpose: To determine the association of demographics, leprosy and ocular characteristics with altered levels of lactoferrin in the tears of normal subjects and leprosy patients, and to detect the presence of antibodies to lactoferrin in these tear samples.
Method: We collected light-stimulated tears from 298 leprosy patients and an equal number of normal subjects using the glass capillary method. Free lactoferrin levels were estimated using ELISA and the presence of antibodies to lactoferrin was detected using the immuno-blotting method. Significant associations were looked for between tear lactoferrin levels and demographic characteristics, leprosy characteristics such as type of disease, duration of disease, reactions, deformity and bacterial load, and ocular complications, using chi-square and regression analysis.
Results: Tear lactoferrin levels with a mean (SD) of 2.55 (2.83)mg/ml in the control group were significantly different (P<0.000) from leprosy patients with a smean (SD) of 5.66 (7.21)mg/ml. Age showed an inverse correlation with tear lactoferrin levels in controls. Increased bacterial load, grade 2 leg deformity and Type 2 reactions were significantly associated (P<0.05) with increased tear lactoferrin levels. Type 2 reactions remained significantly associated ( P=0.01) on multiple regression analysis. Tear lactoferrin levels were not associated with gender, serum lactoferrin levels, Type 1 reactions, face patches, treatment status, orbicularis oculi weakness, lagophthalmos, ectropion, entropion, corneal opacity, cataract and iridocyclitis.
Conclusion: Age is inversely related to tear lactoferrin levels in normal subjects. Free lactoferrin levels in tears are significantly higher in leprosy patients compared with normal controls. Type 2 reactions in leprosy are significantly associated with elevated tear lactoferrin levels.
|How to cite this article:|
Daniel E, Duriasamy M, Ebenezer GJ, Shobhana, Job CK. Elevated free tear lactoferrin levels in leprosy are associated with type 2 reactions.Indian J Ophthalmol 2004;52:51-56
|How to cite this URL:|
Daniel E, Duriasamy M, Ebenezer GJ, Shobhana, Job CK. Elevated free tear lactoferrin levels in leprosy are associated with type 2 reactions. Indian J Ophthalmol [serial online] 2004 [cited 2019 Dec 14 ];52:51-56
Available from: http://www.ijo.in/text.asp?2004/52/1/51/14631
Lactoferrin is a glycoprotein present in exocrine secretions like milk, tears, nasal exudate, saliva, bronchial mucus, gastrointestinal fluids, cervicovaginal mucus and seminal fluid. It is also produced in polymorphonuclear leukocytes. Several studies have shown that lactoferrin has various bactericidal effects. It has exhibited significant activity against Escherichia coli, Proteus mirabilis, Staphyloccocus aureus, Candida albicans and several other bacterial pathogens., Lactoferrin also exhibits immuno-modulatory activities. It is thought to promote the growth and differentiation of T lymphocytes and known to bind uniquely in the region of major histocompatability (MHC) proteins and the CD4 and CD8 determinants on T4 (helper) and T8 (suppressor) lymphocytes. It also appears to play a role in the regulation of cytokines and lymphokines., Lactoferrin levels have been investigated in the tears of diabetics, HIV patients, chronic hepatitis patients, chronic meibonitis associated with acne rosacea and in the tears of contact lens wearers developing giant papillary conjunctivitis.
Lactoferrin levels are raised in lepromatous leprosy patients with Type 2 reactions. This study was done to determine whether tear lactoferrin levels were associated with demography, leprosy and ocular characteristics. Although leprosy is a chronic infectious disease, it is also, to a great extent, considered an immunological disease. Mycobacterium leprae induces a complex humoral and cellular immune response in the host. Documented evidence exists that there is cross-reactivity between human lactoferrin and the 65 kDa heat shock protein of the leprosy bacilli. Since the organism can form immune complexes with the antibody to lactoferrin, we also detected antibodies to lactoferrin in tear samples of patients and controls to determine any association between the presence or absence of antibodies raised against lactoferrin and variables that exist in leprosy and eye complications related to a host-immune response.
Materials and Methods
Patients and Controls
Consecutive leprosy patients admitted as in-patients to the hospital and attending the out-patient department of the Schieffelin Leprosy Research and Training Center, conforming to certain stratifying criteria were invited to participate in the study. The stratification included (1) smear negative leprosy patients who were newly diagnosed, under treatment and released from treatment (RFT), (2) smear positive patients who were newly diagnosed, under treatment and RFT, (3) patients with past and present Type 1 and Type 2 reaction, and (4) patients with eye complications related to leprosy like lagophthalmos and iridocyclitis. An equal number of persons who did not have leprosy but belonged to the same socio-economic status (SES) served as controls. These were selected as much as possible to match the age and gender of patients. Individuals with any ocular abnormalities or any known systemic disease were not included in the control group.
After informed consent was obtained, each of the recruited patients and controls were asked to complete a demography questionnaire. The patients were then assessed for leprosy characteristics that included type of leprosy (categorised according to the Ridley and Jopling classification and the World Health Organization (W.H.O.) treatment classification), the approximate duration of the disease, skin smear positivity for acid fast bacilli, deformity grading (according to the W.H.O. classification), presence or absence of Type 1 or Type 2 reaction, treatment status, relapse, presence or absence of face patch, extra clofazimine therapy and corticosteroid therapy. This was followed by an ocular examination which included specifically checking for madarosis, orbicularis oculi weakness, lagophthalmos, ectropion, entropion, corneal opacity, features of past or present iridocyclitis, naso-lacrimal duct patency and cataract.
Estimation of Free lactoferrin
Tears were collected from the right lower conjunctival sac of patients and controls by stimulating the eyes with a bright light source and using sterile glass capillaries. Tears were taken from the left eye of patients only if a local ocular condition specified as a stratifying criterion warranted such a collection. 5ml of blood was collected by venous puncture with sterile disposable syringes and the serum separated by centrifugation. The collected tears and serum were stored at -20°C till use. Tear and serum lactoferrin were quantified as per the protocol used by Kijlstra et al,16 with following modification. The reaction volume was scaled down to suit the microtitre plates and orthophenylene diamine with 30% hydrogen peroxide was used as substrate instead of ABTS (2-2' - Azino di - (3-ethyl-benzthiazoline - 6 - sulphonate). The competitive binding of anti-human lactoferrin to free lactoferrin in samples against bound lactoferrin was measured and the quantity calculated with the help of a standard graph. Briefly, all the wells except the blank were coated with AQ 100 µl of 0.05µg /ml human milk lactoferrin (Sigma) diluted in coating buffer for 1 hour at 37 °C. Washing of excess lactoferrin was done with 0.1% PBST (0.1% Tween-20 in phosphate buffered saline) thrice. Standards were included in each plate with serially diluted lactoferrin ranging from 0.1µg/ml to 0.0015625µg/ml. Lactoferrin standards and samples were assayed in triplicates. In test wells, 100µl samples of tear at four different dilutions (1:104 to 1:107) and serum 1: 10 and neat were added. Dilutions were made with incubation buffer (3% bovine serum albumin (BSA) in 0.1% PBST). To this 100ul of 1:2000 of rabbit anti human lactoferrin antibody (DAKO A/S Copenhagen, Denmark) prepared in 0.1 % PBST was added and incubated at room temperature on shaker for one hour to facilitate competitive binding. Plates were then washed thrice with 0.1% PBST. 100ul of goat anti rabbit - horseradish peroxidase conjugate (DAKO) diluted 1:2000 with 0.1 % PBST was added and incubated at room temperature for one hour. Excess conjugate was removed by washing thrice with 0.1%PBST. 100 l of freshly prepared Ortho-phenylene diamine (Sigma Chemicals Co, St. Louis, MO, USA ) with 30% H2O2 was added to each well and the plate left in darkness at room temperature for 30 minutes. The reaction was stopped with 100µl of 0.5M sulfuric acid and the Optical density read at 490nm.
Detection of antibody to lactoferrin
Cross reactivity of anti-65kDa antibody was confirmed against heat killed M leprae and purified human lactoferrin. Pooled serum from 10 patients with high bacterial index (BI) and Type 2 reactions was used as positive control. Dot immunoblotting protocol was designed and standardised using the positive controls and was based on a protocol followed in an earlier study.17 Briefly, 5µg of purified human milk lactoferrin mildly denatured with 1 N Sodium hydroxide was blotted to nitrocellulose membrane (Schleicher & Schuell, Inc, Keene, NH, USA) and allowed to air dry. To confirm cross reactivity with M leprae antigens, heat-killed bacilli at a concentration of 1 x 107 per ml was blotted and the membrane blocked with 100µl of 3% BSA in 0.3% Tween 20 in Tris buffered saline (TBST) to prevent nonspecific binding. Tears were diluted to 1:10,000 and incubated with the membrane-bound antigens for an hour at room temperature. Excess tear samples were washed thrice with 0.1% TBS. Antibodies bound to lactoferrin and M.leprae in the membrane were detected using anti-human IgG, IgA and IgM (DAKO) conjugated with alkaline phosphatase. Excess conjugate were washed and the colour developed with 5-Bromo-4-Chloro-3-Indolyl Phosphate/Nitro Blue Tetrazolium substrate. A bluish-violet color indicates the presence of antibodies to lactoferrin. A consensus of four independent observers for the development of colour for both lactoferrin and heat killed M.leprae was considered positive.
Results were entered into an Excel database and simple linear regression and the multiple linear regression analysis using different models were done using the STATA 7.0 package.
Two hundred and ninety eight leprosy patients and an equal number of controls agreed to participate in the study. Their distribution by age and gender is given in [Table 1]. The age of the patients and controls ranged from 15 to 79 years. There were 230 and 226 males in the patient and control group respectively. There was no significant difference in the age or gender of both groups. Regression of tear lactoferrin and age in the control group showed an inverse correlation with a coefficient (SE) of -0.03232 (0.01047) and a 95%C.I. of
-0.0529295 to -0.0117149 (P20 mg/ml and the other with values of 20mg/ml or less. There was significant association (P0.05). The two extreme values were present in young males but otherwise showed no relation to any of the variables.
Tear lactoferrin levels in systemic and ocular diseases have shown varying results. Tear lactoferrin level is reduced in chronic hepatitis C infection and in HIV positive asymptomatic patients., No correlation between lactoferrin content of tears could be demonstrated between normal subjects and diabetics. In our study skin smear results for acid-fast bacilli, both at the time of diagnosis of the disease and the latest results closer to when the tears were collected, were available for all leprosy patients. In patients who showed the presence of acid-fast bacilli, particularly with the BI of 2+ and above, it is likely that the conjunctival and lid tissue had M.leprae in considerable quantities. Increased levels of mycobacteria were significantly associated with increasing levels of lactoferrin.
One other important, consistent, significant, association for increased tear lactoferrin was the Type 2 reaction, also known as Erythema Nodosun Leprosum (ENL). Type 2 reactions occur in lepromatous leprosy, especially in patients with a high load of M leprae . They are characterised by painful and tender nodules on the skin. Apart from the skin lesions they can also cause neuritis, iridocyclitis and orchitis. Immune complexes are formed in these reactions. Histopathologically there is dense infiltration of neutrophils. An earlier study has also shown that serum lactoferrin was raised considerably in lepromatous patients with Type 2 reactions. In our study, patients with Type 2 reactions were 50 times more likely to have significantly raised lactoferrin levels than patients without active Type 2 reaction. The raised levels of lactoferrin in the tears of patients with Type 2 reactions may be a reflection of the neutrophilia present in these patients. It is known that lactoferrin is released from neutrophil granules during inflammation. Lactoferrin in tears is secreted by the lacrimal gland and considered to be a regulated lacrimal gland protein. It is possible that patients with Type 2 reactions also have some amount of dacryoadenitis and the inflammation of the lacrimal glands during the reaction may be responsible for the raised tear lactoferrin levels. Increased levels of tear lactoferrin were not significantly associated in patients with past history of Type 2 reactions suggesting that raised tear lactoferrin levels return to lower normal levels after the acute episode. It is possible that tear lactoferrin has the potential to be a predictive inflammatory marker of Type 2 reactions. Longitudinal follow-up of multi-bacillary leprosy patients and estimation of tear lactoferrin at regular intervals in these patients, including those developing an acute phase of Type 2 reaction, could substantiate this hypothesis.
Iridocyclitis is considered a localised form of Type 2 reaction. It could occur in isolation in lepromatous leprosy patients or as part of the other manifestations of Type 2 reactions. Elevated levels of lactoferrin were not associated with past or present iridocyclitis. Raised lactoferrin levels have been documented in arthritic joint exudates and have been suggested to play a role in inflammations. However, iridocyclitis, although an inflammatory reaction, does not alter the levels of lactoferrin in tears. This is probably because the inflammation is intraocular and not related to the lacrimal glands or the tissues that are directly in contact with the tear film. Local inflammations like chronic meibominitis associated with acne rosacea, contact lens wearers developing giant papillary conjunctivitis, cataract surgery, and keratoconjunctivitis sicca reduce tear lactoferrin levels. Lactoferrin levels were raised in patients who had grade 2 leg deformities. Elevated lactoferrin is demonstrated in neurodegenerative diseases like Alzheimer's disease, Down's syndrome, amyotrophic lateral sclerosis, Parkinsonism-dementia complex of Guam and sporadic amyotrophic lateral sclerosis. An excessive accumulation of lactoferrin, as well as transported iron and aluminum, may lead to a cytotoxic effect resulting in the formation of intracellular lesions and neuronal death. This could account for the association of grade 2 deformities with raised free tear lactoferrin levels.
We did not find a significant difference in the amounts of antibodies to lactoferrin in the tears of leprosy patients as compared to controls. The only variable that was associated significantly with the antibodies to lactoferrin among leprosy patients was increased presence of the leprosy bacilli in the body of these patients. Neither leprosy reactions nor local ocular inflammations showed any relationship to the presence of antibodies to lactoferrin in tears.
Dr. Brennen's laboratory monoclonal antibodies for 65kDa M.leprae antigens. Mr Yowan, Dr Sheena Koshy and Dr Kala Gopalakrishnan recruited and examined the leprosy patients.
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