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Abstrak :
ABSTRAK
Latar Belakang: Penggunaan PRP autologus banyak dimanfaatkan untuk mempercepat proses penyembuhan berbagai macam luka, namun belum ada kriteria yang mengatur penggunaan tersebut. Penelitian yang menjelaskan bagaimana pengaruh penggunaan PRP terhadap proses tersebut juga masih sangat terbatas. Penelitian ini bertujuan untuk mengalisa pengaruh PRP terhadap produksi mediator pro dan anti-inflamasi dari kultur makrofag.Metode: Penelitian eksperimental ini menggunakan sampel darah perifer dari subyek sehat yang diambil sebanyak 2x dengan interval waktu 1 minggu. Pada pengambilan darah pertama, dilakukan isolasi sel monosit kemudian dikultur selama 1 minggu menjadi sel makrofag. Pada hari ke-7 dilakukan pengambilan darah kedua untuk dilakukan isolasi PRP dan serum, kemudian dilakukan 5 kelompok perlakuan berbeda terhadap masing-masing subyek. Kelompok I, makrofag ditambah serum. Kelompok II, makrofag ditambah serum dan LPS. Kelompok III, makrofag ditambah serum, LPS, dan PRP. Kelompok IV, makrofag ditambah LPS dan PRP. Kelompok V, makrofag ditambah PRP. Pada hari ke-10 dan ke-14, kadar sitokin TNF-a dan IL-10 yang dihasilkan dari kultur makrofag diukur dengan menggunakan teknik ELISA.Hasil: Terjadi penurunan bermakna kadar TNF-a hari ke-14 dibandingkan hari ke-10 pada kelompok II p=0.001 , kelompok III p=0.011 , dan kelompok IV p=0.000 . Kemampuan sel makrofag untuk memproduksi TNF-a menurun pada hari ke-14 dibanding hari ke-10. Terjadi peningkatan bermakna kadar IL-10 hari ke-14 dibandingkan hari ke-10 pada kelompok I p=0.05 , kelompok II p=0.018 , kelompok III p=0.017 , kelompok IV p=0.030 , dan kelompok V p=0.030 . Kemampuan sel makrofag untuk memproduksi IL-10 meningkat pada hari ke-14 dibanding hari ke-10, namun tidak ada perbedaan bermakna antar tiap kelompok.Kesimpulan: Secara umum, kadar TNF-a menurun pada hari ke-14 dibandingkan hari ke-10 sedangkan kadar IL-10 meningkat pada hari ke-14 dibandingkan hari ke-10. Pemberian PRP dapat meningkatkan produksi kadar TNF-a pada awal aktivasi makrofag dan menurunkan produksi TNF-a pada akhir aktivasi makrofag. Pemberian PRP tidak mempengaruhi produksi IL-10 pada awal aktivasi makrofag dan meningkatkan produksi IL-10 pada akhir aktivasi makrofag.

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ABSTRACT
Background Autologous PRP has been used widely to accelerate wound healing, but many are case reports lacking controls. Research explains how the effect of the use of PRP to the process is still very limited. This study was aimed to analyze the effect of PRP on the production pro and anti inflammatory mediators from macrophage culture.Methods This experimental research was prepared from peripheral blood samples collected 2 times from healthy subjects, within an interval of 1 week. In the first blood collection, monocytes were isolated then cultured for 1 week into macrophage Human monocyte derived macrophages . On day 7, the second blood collection was done to isolate PRP and serum, then 5 different treatments were treated to each subject. Group I, macrophage plus serum. Group II, macrophage plus serum and LPS. Group III, macrophage plus serum, LPS, and PRP. Group IV, macrophage plus LPS and PRP. Group V, macrophage plus PRP. On day 10 and day 14, cytokine TNF a and IL 10 that produced by macrophage culture were measured using ELISA technique.Results There was significant decrease of TNF a concentration on day 14 compared to day 10, especially in Group II p 0.001 , Group III p 0.011 , and group IV p 0.000 . Macrophage rsquo s ability to produce TNF a was decrease on day 14 compared to day 10. There was significant increase of IL 10 concentration on day 14 compared to day 10, in Group I p 0.05 , Group II p 0.018 , Group III p 0.017 , Group IV p 0.030 , and Group V p 0.030 . Macrophage rsquo s ability to produce IL 10 was increase on day 14 compared to day 10, but there was no significant difference between each group.Conclusions In general, TNF a concentration decrease on day 14 compare to day 10 but IL 10 concentration increase on day 14 compare to day 10. PRP supplement can increase the production of TNF a in the first phase of macrophage activation and reduce the production of TNF a in the late phase of macrophage activation. PRP supplement doesn rsquo t influence the production of IL 10 in the first phase of macrophage activation but can induce the increasing of IL 10 production in late phase of macrophage activation.

Abstrak :
Pada beberapa tahun ini, peningkatan keparahan penyakit kronis dan gangguan kualitas hidup berhubungan dengan kondisi overweight pada orang dewasa dan termasuk dalam chronic low grade Inflamation. Penelitan terhadap kondisi overweight pada orang dewasa dilihat dari sisi imunitas tergambarkan pada beberapa mediator sel imun khususnya sitokin dalam hal ini TNF-α, IL-6 dan IL-10. Sitokin inflamasi pada individu overweight diproduksi berlebih oleh white adipose tissue sehingga terjadi ketidakseimbangan dalam imunitas. Kuesioner Status imun dapat menilai kerentanan seseorang terhadap penyakit yang berhubungan dengan imunitas. Melalui penelitian ini bertujuan menganalisis hubungan mediator inflamasi: TNF-α/IL-10 dengan skor status Imunitas menggunakan kuesioner yang tervalidasi dan membandingkan sitokin tersebut antara kelompok golongan non- dan Overweight -Obesitas. Penelitian ini menggunakan studi potong lintang dengan data kuesioner pada 100 subjek yang diukur serum darah TNFα, IL-10 menggunakan teknik magnetic luminex multiplex immunoassay. Hasil analisa didapatkan perbedaan bermakna antara nilai TNFα di kelompok non- dengan nilai TNFα pada kelompok obese-overweight dengan p= 0.028 (p<0.05) dan pada rasio sitokin tersebut dengan p= 0.032(p<0.05). Hubungan skor ISQ dengan TNFa korelasi p=0.039 (p<0.05). Dapat disimpulkan adanya hubungan bermakna antara TNFα berikut rasionya dengan skor ISQ serta ditemukan kadar TNFα dan rasionya pada kelompok overweigth-obese lebih tinggi dibandingkan dengan kelompok non Overweight -Obesitas ......In recent years, increased severity of chronic disease and impaired quality of life have been associated with overweight in adults and as part chronic low grade inflammation. Research on overweight conditions in adults in terms of immunity is described in several immune cell mediators, especially cytokines in this case TNF-α, IL-6 and IL-10. Inflammatory cytokines in overweight individuals are produced in excess by white adipose tissue, resulting in an imbalance in immunity. The Immune Status Questionnaire can assess a person's susceptibility to immune-related diseases. This study aims to analyze the relationship between inflammatory mediators: TNF-α/IL-10 with Immunity status scores using a validated questionnaire and compare these cytokines between the non- and Overweight-Obesity groups. This study was cross-sectional study with questionnaire data on 100 subjects and blood serum TNFα, IL-10 were measured using magnetic luminex multiplex immunoassay technique. The results of the analysis showed a significant difference between the TNFα in the non-group and the TNFα in the obese-overweight group with p= 0.028 (p<0.05) and the ratio with p= 0.032 (p<0.05). The relationship between ISQ scores and TNFa correlation p=0.039 (p<0.05). It concluded that there is a significant relationship between TNFα and its ratio with ISQ scores and found TNFα levels and ratios in the overweight-obese group were higher than in the non-Overweight-Obesity group

Abstrak :
Telah dilakukan suatu penelitian eksperimental untuk menilai peran sel T regulator pada pasien dengan ko-infeksi HIV-TB. Terhadap 18 subyek HIV positif dilakukan penilaian IGRA, isolasi dan kultur PBMC dengan stimulasi antigen MTB, serta sorting dan deplesi Treg CD4 CD25highCD127low dengan metode FACS. Produksi sitokin IFN- dan IL-10 dinilai secara kuantitatif dengan multiplex Luminex 200. Diperoleh sebanyak 10 55,6 subyek TB negatif, 6 33,3 subyek TB laten, dan 2 11,1 subyekTB aktif. Persentase Treg dari CD4 pada subyek HIV dengan status TB menunjukkan kenaikan signifikan dibanding nilai referensi batas atas persentase Treg dalam CD4 subyek normal 11,006 2,840 ; p=0,008 . Rerata persentase Treg dari sel PBMC total antara kelompok TB aktif dan TB negatif menunjukkan perbedaan yang signifikan 1,3 vs 0,8 ; p=0,036 . Tidak terdapat perbedaan rasio sitokin proinflamasi INF- terhadap sitokin anti inflamasi IL-10 pada kelompok dengan ko infeksi HIV- TB aktif dan laten sebelum dan sesudah deplesi Treg.

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An experimental study has been conducted to assess the role of T regulatory cells in patients with HIV TB co infection. 18 HIV positive subjects undergo IGRA assessment, PBMC isolation and culture with ESAT 6 CFP 10 mycobacterial antigen stimulation, and Treg CD4 CD25highCD127low sorting and depletion by FACS method. The production of cytokines IFN and IL 10 were quantitatively assessed with Luminex 200 multiplex assay. Respectively, 10 55.6 were negative TB subjects, 6 33.3 were latent TB subjects, and 2 11.1 subjects were TB active. The percentage of Treg from CD4 cells in HIV subjects with TB status showed a significant increase over the reference value in normal subjects 11.006 2.840 p 0.008 . The mean percentage of Treg from total PBMC cells between active and negative TB groups showed a significant difference 1.3 vs. 0.8 p 0.036 . There was no difference in the ratio of proinflammatory cytokines INF to the anti inflammatory cytokine IL 10 in the group with active and latent HIV TB infection coinfection before and after Treg depletion.

Abstrak :
Latar belakang: Periodontitis merupakan inflamasi kronis yang dapat merusak jaringan periodontal dan mempengaruhi hinggi 50% populasi dunia, sedangkan prevalensinya di Indonesia sebesar 77,8%. Perubahan pada proses inflamasi di jaringan periodontal terjadi akibat faktor mikrobial yang mengubah ekspresi faktor-faktor inflamasi seperti IL-1, TNF-, IL-6, IL-10. Konjac glucomannan (KGM) adalah polisakarida dari tanaman Amorphophallus konjac, yang sudah lama dikonsumsi sebagai sumber makanan dan obat tradisional. Banyak penelitian menunjukkan kemampuan KGM untuk memodulasi reaksi inflamasi, yang berpotensi untuk pencegahan dan perawatan penyakit periodontal. Tujuan: Mendapatkan efek anti-inflamasi KGM secara histologis (skor dan distribusi) dan biomolekuler (kadar IL-6 dan IL-10 di gingival crevicular fluid/GCF dan serum) pada model periodontitis di mencit Swiss Webster. Metode: Mencit Swiss Webster berusia 8 minggu dibagi secara acak ke dalam empat kelompok perlakuan (Kontrol, Konjac, Periodontitis, Periodontitis+Konjac). Suspensi KGM diberikan selama 14 hari dan induksi periodontitis dilakukan tujuh hari setelah pemberian KGM. Euthanasia dilakukan setelah 14 hari penelitian dan diambil sampel GCF, serum dan maksila mencit untuk pembuatan preparat histologis. Hasil: Kelompok periodontitis menunjukkan skor dan distribusi inflamasi tertinggi dan menurun setelah pemberian KGM. Pemberian KGM pada mencit periodontitis dapat mencegah penurunan kadar IL-10 serum dan peningkatan kadar IL-6 serum. Pemberian konjac pada mencit sehat cenderung meningkatkan kadar IL-6 GCF dan IL-10 GCF, walaupun tidak berbeda secara statistik. Kesimpulan: Pemberian KGM mampu menurunkan tingkat inflamasi pada model periodontitis secara histologis dan mengubah proses inflamasi. ......Background: Periodontitis is chronic inflammation that characterized by the destruction of periodontal tissue, affecting up to 50% of the world’s population and having a prevalence as high as 77.8% in Indonesia. The inflammatory process in periodontal tissue changes as a result of microbial factors that will affect the expression of pro- and anti-inflammatory factors such as IL-1, TNF-, IL-6, IL-10. Konjac glucomannan (KGM) is a polysaccharide from the tubers of Amorphophallus konjac, that have long been used as a food source and traditional Chinese medicine. Many studies have shown that KGM is capable of modulating inflammation, which has potential usage for the prevention and treatment of periodontal diseases. Aim: To study anti-inflammatory effects of KGM thru histological (score and distribution) and biomolecular (levels of IL-6 and IL-10 in gingival crevicular fluid and serum) analysis on periodontitis model in Swiss Webster mice. Methods: Eight weeks old mice is randomly divided into four groups (Control, Konjac, Periodontitis, Periodontitis+Konjac). Konjac glucomannan suspension is administered daily for 14 days dan mice is ligated to induce periodontitis 7 days after administration of KGM. Mice is euthanized after 14 days and GCF, serum and maxilla is acquired for analysis. Results: Periodontitis group have the highest inflammation score and distribution out of all the groups and reduces with administration of KGM. Administration of konjac glucomannan prevents the reduction of IL-10 serum levels and increase of IL-6 serum levels in mice with periodontitis. While KGM increases both IL-6 and IL-10 GCF levels in healthy mice, though not statistically significant. Conclusion: Adminstration of KGM can supress inflammation in mice periodontitis model histologically and alter the inflammatory process.

Abstrak :
Endometriosis merupakan penyakit ginekologi umum yang dipicu terjadinya peradangan kronis yang ditandai dengan produksi beberapa sitokin pro-inflamasi, salah satu yang terbanyak yaitu TNF-α. Di sisi lain, sitokin anti-inflamasi, seperti IL-10, dapat mengakhiri proses inflamasi berlanjut ini. Propolis adalah bahan bioaktif alami produk lebah, sebagai imunomodulator dan efek anti-inflamasi yang dapat menekan proliferasi sel-sel patologis. Penelitian ini bertujuan untuk menentukan pengaruh pemberian propolis terhadap tumor necrosis factor alpha dan interleukin 10. Penelitian ini menggunakan desain uji klinis dengan alokasi acak dan double-blinded. 24 wanita dengan terapi Levonorgestrel (LNG) karena endometriosis secara acak ditugaskan untuk menerima propolis yang mengandung 17,5 mg flavonoid per tetes atau plasebo. Intervensi diberikan dua kali sehari, pada pagi dan malam hari, dengan dosis 1 tetes/10 kg berat badan (kgBB) per kali. Sampel darah dan penilaian gizi diambil pada kunjungan pertama dan 30 hari setelahnya. Hasil penelitian menunjukkan bahwa kadar tumor necrosis factor alpha dan interleukin 10 tidak memiliki perbedaan yang signifikan antara kedua kelompok (p>0,05). Kadar tumor necrosis factor alpha mengalami penurunan yang lebih besar pada kelompok propolis sebesar 4,17 (44,36-50,05) pg/mL dibandingkan dengan kelompok plasebo. Kadar IL-10 menunjukkan peningkatan sebesar 344,94 setelah 30 hari diberikan intervensi. Pemberian flavonoid dalam propolis tidak menghasilkan perubahan yang signifikan dalam kadar Tumor Necrosis Factor Αlpha dan Interleukin 10 selama periode intervensi 30 hari. ......Endometriosis is a common gynecological disease triggered by chronic inflammation characterized by the production of several pro-inflammatory cytokines, one of which is TNF-α. On the other hand, anti-inflammatory cytokines, such as IL-10, can end this ongoing inflammatory process. Propolis are natural bioactive ingredients contained in bee products, as immunomodulators and anti-inflammatory effects that can suppress the proliferation of pathological cells. This study aimed to determine the effect of propolis supplementation on tumor necrosis factor alpha and interleukin 10. This study used clinical trial design with random allocation and double- blinded. 24 women with Levonorgestrel (LNG) therapy due to endometriosis were randomly assigned to receive propolis-contained 17.5 mg of flavonoids per drop or placebo. The intervention given two times a day,in the morning and at night, with a dose of 1 drop /10 kg body weight (kgBW) per time. Blood samples and nutritional assessment were taken at the first time of visit and 30 days thereafter. The results showed that the levels of tumor necrosis factor alpha and interleukin 10 did not differ significantly between the two groups (p>0.05). Tumor necrosis factor alpha levels experienced a greater decrease in the propolis group by 4.17 (44.36-50.05) pg/mL compared to the placebo group. IL-10 levels showed an increase of 344.94 after 30 days of intervention. The administration of propolis supplementation did not result in significant changes in the levels of Tumor Necrosis Factor Αlpha and Interleukin 10 during the 30- day intervention period.

Abstrak :
Kondisi hipoksia hipobarik dapat mengganggu kesehatan manusia dan menjadi risiko keselamatan di dunia penerbangan. Berbagai jalur pensinyalan sensitif oksigen pada tingkat seluler, dapat diaktifkan selama paparan hipoksia hipobarik intermiten (HHI). HSP sebagai chaperokine berperan dalam transduksi sinyal dan modulasi sistem imun serta terkait dengan produksi sitokin pro-inflamasi atau anti-inflamasi. Penelitian ini bertujuan menganalisis efek HHI terhadap HSP70 dan produksi sitokin pro dan anti-inflamasi. Penelitian ini merupakan penelitian eksperimental dengan menggunakan jaringan hepar tikus Sprague-Dawley yang disimpan pada suhu -20°C. Tikus dibagi menjadi 5 kelompok yaitu kontrol (C), HHA, HHI1, HHI2, dan HHI3 dan diberikan paparan HHI pada ketinggian 25.000 kaki selama 5 menit. Analisis konsentrasi protein dan sitokin ditentukan dengan metode sandwich ELISA. Hasil penelitian menunjukkan terdapat perbedaan bermakna ekspresi protein HSP70 pada hepar tikus pada kelompok HHA dan HHI terhadap kontrol (p<0.05), terdapat perbedaan bermakna konsentrasi IL-10 antara kelompok HHI3 terhadap kontrol (p = 0,018), dan adanya korelasi positif dengan kekuatan korelasi sedang antara HSP70 dengan TNF-α dan IL-1β, serta korelasi positif sedang HSP70 dengan IL-10. HHI menginduksi peningkatan HSP70 sebagai mekanisme adaptasi dan memodulasi sistem imun tubuh untuk meningkatkan konsentrasi IL-10. ......Hypobaric hypoxic conditions can disrupt human health and become a risk for safety of aviation. Various signaling oxygen-sensitive pathways at the cellular level can be activated during intermittent hypobaric hypoxia (IHH) exposure. HSP as a chaperokine plays a role in signal transduction and modulation of the immune system and it is associated with the production of pro-inflammatory or anti-inflammatory cytokines. This study aims to analyze the effect of IHH on HSP70 and the production of pro- and anti-inflammatory cytokines. This study was an experimental study using Sprague-Dawley rat liver tissue stored at -20°C. Rats were divided into 5 groups, they are control (C), AHH, IHH1, IHH2, and IHH3. They were exposed to IHH at altitude of 25,000 feet for 5 minutes. Analysis of protein and cytokines concentrations was determined by the sandwich ELISA method. The results showed that there was a significant difference in HSP70 protein expression in the liver of rats in the HHA and IHH groups compared to the control (p<0.05), there was a significant difference in IL-10 concentration between the IHH3 group compared to the control (p = 0.018), a positive correlation with moderate correlation strength between HSP70 with TNF-α and IL-1β, and a moderate positive correlation between HSP70 with IL-10. HHI produces an increase in HSP70 as an adaptive mechanism and modifies the immune system to raise the levels of IL-10.

Abstrak :
[ABSTRAK
Kemampuan Mycobacterium tuberculosis yang dapat memanipulasi dan menghindari respon imun adalah tantangan dalam mencari terapi dan vaksinasi efektif. Penelitian ini untuk menguji potensi ekstrak metanol akar Eurycoma longifolia Jack dalam memodulasi peningkatan IgA dan IgG mencit putih jantan yang divaksinasi BCG, sekaligus untuk menganalisis peningkatan sitokin proinflamasi yang berhubungan dengan produksi IgA dan IgG. Plasma diambil sebelum dan setelah vaksinasi BCG pada 18 ekor mencit yang dibagi ke dalam 2 kelompok; perlakuan dan kontrol. Kadar IgA, IgG, TNF-! dan IL-10 diukur dengan metode ELISA. Hasil menunjukkan bahwa peningkatan IgA kelompok air (0,33±0,16) lebih tinggi dibandingkan kelompok pasak bumi (0,30±0,30), sedangkan peningkatan IgG kelompok pasak bumi (0,38±0,25) terlihat lebih tinggi dibandingkan kelompok air (0,29±0,35). Rasio TNF-!/IL-10 kelompok pasak bumi (0,46±0,07) lebih tinggi dibandingkan kelompok air (0,41±0,05). Terdapat korelasi antara TNF-! dengan IgA pada kelompok air (r=0,601, p=0,035) juga dengan IgG pada kelompok pasak bumi (r=0,559, p=0,059). Disimpulkan, pemberian pasak bumi cenderung berpotensi memodulasi peningkatan IgG, tetapi tidak IgA. Selain itu, pemberian pasak bumi juga cenderung meningkatkan sitokin proinflamasi yang mempengaruhi produksi IgA dan IgG.

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ABSTRACT
The ability of Mycobacterium tuberculosis to manipulate and evade host?s immune response is a challenge in finding an effective therapy and vaccination. The purpose of this research were to investigate the potency of methanol extract of the roots of Eurycoma longifolia Jack as immunomodulators for male white mice vaccinated with BCG, as well as to analyze the increase of proinflammatory cytokines associated with IgA and IgG production. Plasma were taken before and after BCG vaccination from 18 mice, that were divided into 2 groups; treatment and control. IgA, IgG, TNF-! and IL-10 levels were measured by using ELISA. The results showed that the enhancement of IgA group with water (0,33±0,16) was higher than group with pasak bumi (0,30±0,30). On the other hand the enhancement of IgG group with pasak bumi (0,38±0,25) was higher than group with water (0,29±0,35). The ratio of TNF-!/IL-10 group with pasak bumi (0.46±0.07) was higher than group with water (0.41±0.05). There are correlarions between TNF-! and IgA in the group with water (r=0.601, p=0.035) as well as between TNF- ! and IgG in group with pasak bumi (r=0.559, p=0.059). As the conclusion, methanol extract of pasak bumi root tend to potentially modulate the increase IgG production, but not IgA. In addition, it also tends to increase the proinflamasi cytokines associated with IgA and IgG production.;The ability of Mycobacterium tuberculosis to manipulate and evade host’s immune response is a challenge in finding an effective therapy and vaccination. The purpose of this research were to investigate the potency of methanol extract of the roots of Eurycoma longifolia Jack as immunomodulators for male white mice vaccinated with BCG, as well as to analyze the increase of proinflammatory cytokines associated with IgA and IgG production. Plasma were taken before and after BCG vaccination from 18 mice, that were divided into 2 groups; treatment and control. IgA, IgG, TNF-! and IL-10 levels were measured by using ELISA. The results showed that the enhancement of IgA group with water (0,33±0,16) was higher than group with pasak bumi (0,30±0,30). On the other hand the enhancement of IgG group with pasak bumi (0,38±0,25) was higher than group with water (0,29±0,35). The ratio of TNF-!/IL-10 group with pasak bumi (0.46±0.07) was higher than group with water (0.41±0.05). There are correlarions between TNF-! and IgA in the group with water (r=0.601, p=0.035) as well as between TNF- ! and IgG in group with pasak bumi (r=0.559, p=0.059). As the conclusion, methanol extract of pasak bumi root tend to potentially modulate the increase IgG production, but not IgA. In addition, it also tends to increase the proinflamasi cytokines associated with IgA and IgG production., The ability of Mycobacterium tuberculosis to manipulate and evade host’s immune response is a challenge in finding an effective therapy and vaccination. The purpose of this research were to investigate the potency of methanol extract of the roots of Eurycoma longifolia Jack as immunomodulators for male white mice vaccinated with BCG, as well as to analyze the increase of proinflammatory cytokines associated with IgA and IgG production. Plasma were taken before and after BCG vaccination from 18 mice, that were divided into 2 groups; treatment and control. IgA, IgG, TNF-! and IL-10 levels were measured by using ELISA. The results showed that the enhancement of IgA group with water (0,33±0,16) was higher than group with pasak bumi (0,30±0,30). On the other hand the enhancement of IgG group with pasak bumi (0,38±0,25) was higher than group with water (0,29±0,35). The ratio of TNF-!/IL-10 group with pasak bumi (0.46±0.07) was higher than group with water (0.41±0.05). There are correlarions between TNF-! and IgA in the group with water (r=0.601, p=0.035) as well as between TNF- ! and IgG in group with pasak bumi (r=0.559, p=0.059). As the conclusion, methanol extract of pasak bumi root tend to potentially modulate the increase IgG production, but not IgA. In addition, it also tends to increase the proinflamasi cytokines associated with IgA and IgG production.]

Abstrak :
Latar belakang. Graves? Disease (GD) merupakan penyakit autoimun yang paling banyak menyebabkan hipertiroidisme dan ditandai adanya autoantibodi terhadap reseptor hormon tiroid (TSHR). Sel dendritik (DC) berperan penting dalam menentukan jenis respon imun tubuh, berupa aktivasi atau toleransi, salah satunya dengan cara mensekresikan mediator yang dapat mempengaruhi kerja sel-sel lain. Vitamin D merupakan imunoregulator alami yang dalam kondisi normal dapat mempengaruhi DC untuk mensekresikan IDO dan IL-10 serta menekan sekresi IL-12 dari DC. Sekresi IDO dan IL-10 oleh DC dapat mencetuskan respon toleransi dengan meningkatkan aktivitas sel T regulatori (Treg) dalam mencegah dan/atau mengurangi produksi autoantibodi terhadap TSHR. Belum diketahui apakah pemberian vitamin D pada kondisi GD dapat meningkatkan sekresi IDO dan IL-10 serta menekan sekresi IL-12. Tujuan. Melihat pengaruh kadar vitamin D terhadap fungsi DC dan sistem imun pasien GD dalam mensekresikan IL-12, IDO dan IL-10. Metode. Sampel merupakan bahan biologis tersimpan yang berupa supernatan kultur DC dari monosit (kultur MDDC) dan serum dari pasien GD. Kultur MDDC dari pasien GD sebelum perlakuan, diberi pendedahan tanpa atau dengan 1,25(OH)2D3 100 nM, waktu inkubasi 7 hari, dengan penambahan lipopolisakarida (LPS) pada hari ke-5. Kultur MDDC dari pasien GD setelah perlakuan, diinkubasi tanpa 1,25(OH)2D3 selama 7 hari dengan pemberian LPS pada hari ke-5. Serum berasal dari pasien GD sebelum dan sesudah mendapatkan terapi standar PTU 100 mg 3 kali sehari dengan atau tanpa suplementasi 1α(OH)D3. Serum dan supernatan diuji dengan metode ELISA untuk mengukur kadar 25(OH)D3, IL-12, IDO dan IL-10, kemudian diuji secara statistik untuk melihat pola dari tiap parameter. Hasil. Rerata kadar IL-12 lebih rendah secara signifikan pada kultur MDDC dengan pemberian vitamin D 100 nM. Rerata kadar IDO dan IL-10 cenderung tetap pada kultur MDDC dengan pemberian vitamin D 100 nM. Peningkatan kadar vitamin D dalam serum berkorelasi negatif dengan kadar IL-12 dan IDO, baik dalam supernatan kultur MDDC maupun dalam serum pasien GD. Pada kelompok pasien GD dengan peningkatan kadar vitamin D serum tinggi, respon sekresi IL-10 pada MDDC dan sistem imun pasien GD cenderung meningkat. Semakin tinggi rasio kadar IL-12/IL-10 pada supernatan kultur MDDC dan serum pasien GD, maka semakin tinggi juga kadar IDO yang disekresikan. Simpulan. Pemberian vitamin D pada kultur MDDC dari pasien GD dapat menekan respon inflamasi MDDC dengan mengurangi sekresi kadar IL-12 dan mempertahankan kadar IDO dan IL-10. Peningkatan kadar vitamin D serum dapat menekan kadar IL-12 dan IDO, juga berpotensi meningkatkan kadar IL-10, baik pada keadaan in vitro maupun in vivo. ...... Background. Graves' disease (GD) is a type of autoimmune disease that causes hyperthyroidism. GD patients have excess autoantibodies specific for thyroid stimulating hormone receptors (TSHR). Dendritic cells (DCs) play an important role in determining the type of immune response, either activation or tolerance, by secreting mediator molecules that affect other cells. Vitamin D is a natural immunoregulator which in normal condition can affect IDO and IL-10 secretion by DC while suppresing IL-12 secretion by this cell. Secretion of IDO and IL-10 by DC can trigger tolerance by increasing regulatory T cells (Treg) activity in preventing and/or reducing the production of autoantibodies against TSHR. There is still no evidence whether administration of vitamin D at GD conditions can increase the secretion of IDO and IL-10 and suppress the secretion of IL-12. Aim. To identify the effect of vitamin D in vitro and in vivo on IL-12, IDO and IL-10 secretion by DC and on the immune system of GD patients. Method. Samples were stored biological liquid in the form of serum and monocyte derived dendritic cells (MDDC) culture supernatant from GD patients. MDDC cultures of pre-treatment GD patients were incubated for 7 days with or without 1,25(OH)2D3 100 nM, with an addition of LPS on day 5. MDDC cultures of post-treatment GD patients were incubated without 1,25(OH)2D3 for 7 days, with an addition of LPS on day 5. Serum were obtained from GD patients before and after standard therapy of 100mg PTU 3 times a day with or without 1α(OH)D3 supplementation. Levels of 25(OH)D3, IL-12, IDO and IL-10 in the serum and supernatant were measured by ELISA and the results were statistically analyzed to see the pattern of each parameter. Results. The mean levels of IL-12 are significantly lower in MDDC culture with 100 nM vitamin D. The mean levels of IDO and IL-10 in MDDC cultures with 100 nM vitamin D are maintained at the same levels with MDDC without vitamin D. Increased levels of vitamin D in serum is negatively correlated with IL-12 and IDO levels, both in the MDDC supernatant and in the serum of GD patients. In the high-increment-serum-vitamin-D-level group of GD patients, IL-10 secretion in vitro and in vivo tends to increase. Higher ratio of IL-12/IL-10 levels affects an increase in IDO secretion, both in MDDC culture and in patient?s serum. Conclusion. Vitamin D exposure in MDDC culture of GD patients can suppress the inflammatory response by reducing IL-12 secretion and maintaining IDO and IL-10 levels. Increased vitamin D serum level can suppress IL-12 and IDO levels and is also potential in increasing IL-10 level, both in vitro and in vivo.

Abstrak :
ABSTRAK Nama : Imelda Selvine Wantania Program Studi : Magister Kedokteran Kerja Judul : Pengaruh Pemberian Latihan Fisik Submaksimal Akut Prapenyelaman Tunggal Dekompresi terhadap Perubahan Kadar Interleukin-10 pada Penyelam Laki-Laki Terlatih. Latar Belakang : Gelembung gas yang terdapat dalam pembuluh darah dan jaringan tidak selalu merupakan penyebab penyakit dekompresi. Penyakit dekompresi dapat juga disebabkan oleh disfungsi endotel dengan hilangnya hemostasis endotel yang disebabkan oleh reaksi inflamasi saat di kedalaman. IL-10 adalah sitokin antiinflamasi dan merupakan antioksidan yang dapat mencegah reaksi inflamasi. Tujuan penelitian ini untuk membuktikan bahwa latihan fisik submaksimal yang dilakukan 24 jam sebelum penyelaman dapat mencegah penurunan IL-10 akibat penyelaman. Metode : Penelitian ini menggunakan disain eksperimen murni dengan subyek penyelam laki-laki terlatih yang terbagi dua kelompok yaitu kelompok perlakuan dan kontrol. Kelompok perlakuan melakukan latihan fisik submaksimal 24 jam sebelum penyelaman tunggal dekompresi 280 kPa dengan bottom time 80 menit. Kelompok kontrol hanya melakukan penyelaman tunggal dekompresi 280 kPa dengan bottom time 80 menit. Pemeriksaan kadar IL-10 dilakukan tiga kali yaitu awal penelitian, sebelum dan sesudah penyelaman. Hasil : Latihan fisik submaksimal akut yang dilakukan 24 jam sebelum penyelaman tunggal dekompresi efektif mencegah penurunan kadar IL-10 setelah penyelaman pada kelompok perlakuan dengan rerata awal penelitian 0,36 0,08-0,98 pg/ml dan sesudah penyelaman 0,36 0,08-0,98 pg/ml p=0,065 . Pada kelompok kontrol terjadi penurunan kadar IL-10 dengan rerata awal penelitian 0,61 0,21 pg/ml dan sesudah penyelaman 0,39 0,21 pg/ml p=0,000 . Kesimpulan : Latihan fisik submaksimal yang dilakukan 24 jam sebelum penyelaman tunggal dekompresi dapat mencegah penurunan IL-10 setelah penyelaman. Dilain pihak, pada subyek yang tidak melakukan latihan fisik submaksimal 24 jam sebelum penyelaman terjadi penurunan IL-10.

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ABSTRACT Name Imelda Selvine Wantania Study Programe Master of Occupational Medicine Title Effect Of Acute Submaximal Exercise Pre Single Decompression Dive on Changes in IL 10 Consentration In Trained Male Divers Background Gas bubbles contained in the blood vessels and tissues is not always the cause of decompression sickness. Decompression illness can also caused by endothelial dysfunction with loss of endothelial hemostasis caused by an inflammatory reaction when at depth. IL 10 is an anti inflammatory cytokine and antioxidant that prevent inflammatory reaction. The purpose of this study to prove that physical exercise submaximal done 24 hours before the decompression dive can prevent a decrease in IL 10. Methods This research uses pure experimental design with trained male divers as a subject who were split into two groups, treatment and control. Treatment group perform acute submaximal exercise 24 hours before single decompression dives 280 kPa with the bottom time of 80 minutes and the control group dive without perform an acute submaximal exercise but do single dive decompression. Assessment of the level of IL 10 conducted three times, at the beginning of the study, before and after the dive. Result Acute submaximal exercise conducted 24 hours before a single decompression dive effectively prevent IL 10 decrease levels after dive in treatment group with the early treatment group average research 0.36 0.08 0.98 pg ml and after dive 0.36 0.08 0.98 pg ml p 0,065 . In the control group, decreased levels of IL 10 with the early treatment average research 0,61 0.21 pg ml and 0.39 0.21 pg ml dives after p 0.000 . Conclusion Submaximal physical exercise done 24 hours before a single decompression dive can prevent a decrease in IL 10 after dive. The dive performed without submaximal physical exercise before diving decreased IL 10. Keyword single decompression dive IL 10 acute submaximal physical exercise.

Abstrak :
Endometriosis merupakan penyakit ginekologi yang ditandai dengan pertumbuhan jaringan mirip endometrium di luar rongga uterus. Inflamasi kronik pada endometriosis memiliki peranan penting dalam memfasilitasi perkembangan kista endometriosis. Penelitian ini bertujuan untuk menganalisis efektivitas oktil galat dalam menurunkan inflamasi pada tikus Wistar model endometriosis. Sejumlah 30 ekor tikus wistar betina dibagi secara acak ke dalam tiga kelompok. Kelompok pertama dan kedua direkayasa membentuk jaringan endometriosis, sedangkan kelompok ketiga dilaparatomi sebagai kelompok kontrol negatif. Setelah dua bulan, dilakukan laparatomi kedua pada kelompok satu dan dua untuk mengevaluasi pembentukan jaringan endometriosis. Induksi oktil galat diberikan pada kelompok pertama selama satu bulan. Seluruh tikus kemudian dieuthanasia dan jaringan endometriosis kelompok pertama dan kedua, serta jaringan endometrium kelompok ketiga, diambil untuk dianalisis. Pengukuran kadar sitokin TNF-α dan IL-10 dilakukan menggunakan Luminex Multiplex Assay, sedangkan kadar COX-2 dan PGE₂ diukur menggunakan metode ELISA. Analisis beda proporsi menunjukkan bahwa pemberian oktil galat pada kelompok pertama tidak memberikan perubahan kadar TNF-α kategori tinggi yang signifikan, sedangkan kadar COX-2, PGE₂, dan IL-10 kategori tinggi teramati mengalami penurunan signifikan sebesar 22,3%, 55,6%, dan 44,5%, dibandingkan dengan kelompok kedua (p<0,05). Oktil galat diketahui efektif dalam menurunkan mediator inflamasi COX-2 dan PGE₂, serta anti-inflamasi IL-10, yang memicu perbaikan gejala klinis berupa regresi ukuran kista endometriosis. ......Endometriosis is a gynecological disease, characterized by the growth of endometrial-like tissue outside the uterine cavity. Chronic inflammation in endometriosis has an important role in facilitating the development of endometriosis cysts. The present study aimed to analyze the anti inflammatory effect of octyl gallate in endometriosis Wistar rat model. 30 female Wistar rats were divided randomly into three groups. Endometriosis induction was performed in the first and second group, while a sham operation was performed in the third group. Two months later, a second laparotomy was performed in the first and second groups to evaluate endometriosis tissue formation. Octyl gallate was administered via oral gavage to the first group for one month. All rats were sacrificed and endometriosis tissue samples were collected for further analysis. TNF-α and IL-10 levels were measured using Luminex Multiplex Assay, while COX-2 and PGE₂ levels were measured using the ELISA method. The administration of octyl gallate in the first group did not significantly effect TNF-α levels, whereas the high category of COX-2, PGE₂, and IL-10 levels were observed to experience a significant decrease up to 22.3%, 55.6%, and 44.5% compared to the second group (p<0.05). In conclusion, octyl gallate was able to supress the inflammatory mediators, COX-2 and PGE₂, along the anti-inflammatory mediators IL-10, which induced the regression of endometriosis cysts size as an improvement of clinical symptoms.