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All Journal Journal of Tropical Life Science : International Journal of Theoretical, Experimental, and Applied Life Sciences Jurnal Kedokteran Brawijaya Majalah Kedokteran Bandung The Journal of Experimental Life Sciences (JELS) e-Journal Pustaka Kesehatan Research Journal of Life Science Journal of Agromedicine and Medical Sciences Mutiara Medika: Jurnal Kedokteran dan Kesehatan UNEJ e-Proceeding Sari Pediatri Universa Medicina Majalah Kesehatan FKUB Advances in Food Science, Sustainable Agriculture and Agroindustrial Engineering (AFSSAAE) Indian Journal of Forensic Medicine & Toxicology CRJIM (Clinical and Research Journal in Internal Medicine) Lux Mensana: Journal of Scientific Health Jurnal Penelitian IJRETINA - International Journal of Retina

Loeki Enggar Fitri

Universitas Brawijaya

Author-ID : 266832

Agriculture, Biological Sciences & Forestry Biochemistry, Genetics & Molecular Biology Education Engineering Environmental Science Health Professions Immunology & microbiology Industrial & Manufacturing Engineering Library & Information Science Mechanical Engineering Medicine & Pharmacology Neuroscience Nursing Public Health Other

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Deteksi Protein 270 kDa Plasmodium falciparum Isolat Malang pada Membran Eritrosit Penderita Malaria dengan Komplikasi Dewi Indiastari; Sri Winarsih; Loeki Enggar Fitri
Pustaka Kesehatan Vol 6 No 2 (2018)
Publisher : UPT Percetakan dan Penerbitan Universitas Jember

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.19184/pk.v6i2.7785

Erythrocyte which is infected by Plasmodium falciparum will have various changes on its architecture, affinity, and biomolecular. Beside that, the infected erythrocyte also forms a knob at its surface. This knob are contained with various parasite proteins, one of them is Plasmodium falciparum erythrocyte membrane protein-1 (PfEMP-1). Our previous study had been identified a protein with molecular weight 270 kDa at P. falciparum infected erythrocyte from Malang isolate that was playing a role in cytoadherence process. The aim of this study was to detect the possibility of 270 kDa protein expression at complicated malaria falciparum patient erythrocyte membrane. The method that used was immunocytochemistry with polyclonal antibody to 270 kDa protein. The results showed that two (2) erythrocyte samples from healthy people as control had negative reaction, and so did with five (5) erythrocyte samples of uncomplicated malaria patient, but there was positive reaction that shown at two (2) samples of complicated malaria patient erythrocyte. It can be concluded from the results that 270 kDa membrane protein of P. falciparum infected erythrocyte in complicated malaria patient might be a PfEMP-1. This protein can be detected by immunocytochemistry method using polyclonal antibody and can be used for the candidate of complicated malaria diagnostic Keywords: Plasmodium falciparum, 270 kDA protein, immunocytochemistry, polyclonal antibody

Uji Knockdown Effect Ekstrak Bunga Syzygium aromaticum L. terhadap Nyamuk Culex Sp. Dewasa Hayu Sukowati Nopitasari; Loeki Enggar Fitri; Nurdiana Nurdiana
Mutiara Medika: Jurnal Kedokteran dan Kesehatan Vol 14, No 1 (2014): January
Publisher : Universitas Muhammadiyah Yogyakarta

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.18196/mmjkk.v14i1.2473

Nyamuk Culex sp. merupakan vektor penyakit Filariasis, Japanese encephalitis dan demam chikungunya. Insektisida dipilih untuk mengontrol populasi Culex sp. namun, penggunaan insektisida menimbulkan resistensi nyamuk dan efek toksik pada manusia. Oleh karena itu, diperlukan adanya insektisida yang lebih aman bagi lingkungan. Salah satunya adalah dengan menggunakan ekstrak bunga cengkeh (Syzygium aromaticum L.) yang mengandung carvone, terpinen-4-ol, fenchone, eugenol dan quercetine yang berpotensi sebagai insektisida. Tujuan dari penelitian ini adalah untuk membuktikan bahwa ekstrak bunga S. aromaticum L. memiliki knockdown effect terhadap nyamuk Culex sp. Penelitian ini merupakan penelitian eksperimental laboratoris dengan rancangan true experimental-post test only control group design. Sampel yang digunakan adalah 25 ekor nyamuk Culex sp. pada setiap perlakuan. Konsentrasi ekstrak bunga S. aromaticum L. yang digunakan adalah 1,25%, 2,5%, 5% dan sebagai kontrol negatif digunakan larutan aseton 1% serta malathion 0,28% sebagai kontrol positif. Dari uji Kruskal-Wallis diketahui bahwa ekstrak bunga S. aromaticum L. pada menit ke-5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55 dan 60 memberikan perbedaan yang signifikan diantara konsentrasi 1,25%, 2,5%, 5% dan malathion 0,28% (p0,05). Uji korelasi Spearman membuktikan adanya hubungan yang kuat antara knockdown effect dengan besarnya konsentrasi ekstrak bunga S. aromaticum L. (p=0,000 dan r=0,907). Disimpulkan bahwa ekstrak bunga S. aromaticum L. memiliki knockdown effect terhadap nyamuk Culex sp. dewasa.Culex is vector for Filariasis, Japanese encephalitis and Chikungunya fever. Insecticide is chosen to control Culex sp. population. However, the usage of chemical insecticides make insecticide resistant and toxic effect. Therefore, safer alternative insecticide for environment is needed. One of them is by using clove bud extract. Previous studies has proved that clove bud extract (Syzygium aromaticum L.) has containing carvone, terpinen-4-ol, fenchone, eugenol and quercetine a potency to be insecticide on Culex sp. The purpose of this experiment is to prove whether S. aromaticum L. bud extract has knokdown effect on Culex sp. This research was a laboratorial experimental research using true experimental post test only control group design. The samples were 25 Culex sp. in every group which treated by S. aromaticum L. bud extract (1,25%, 2,5%, 5%) and aceton preparation (1%) as a negative control, malathion preparation (0,28%) as a positive control. Kruskal-Wallis test showed that S. aromaticum L. bud extract in 5, 10, 15, 20, 25, 30, 35, 40, 45, 50, 55 and 60 minute gave significant difference among concentration 1,25%, 2,5% and 5% (p0,05). Spearman corelation test prove that there was a significant relationship between knockdown effect produced and the concentration of the S. aromaticum L. bud extract (p=0,000 and r=0,907). It can be concluded that S. aromaticum L. bud extract has knockdown effect against adult Culex sp.

Imunogenic Protein of Salivary Gland from Anopheles sundaicus Yunita Armiyanti; Moh Mirza Nuryady; Sugeng Setyo Utomo; Teguh Wahju Sardjono; Loeki Enggar Fitri; Kartika Senjarini
UNEJ e-Proceeding Indonesian Protein Society (IPS), International Seminar and Workshop 2014
Publisher : UPT Penerbitan Universitas Jember

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Malaria is still a major problem for developing countries, including Indonesia. One approach to overcome this disease is prevention by vaccination. However, there is still no effective malaria vaccine that is applicable. The ideal malaria vaccine is a combination vaccine that can prevent the pre-erythrocytic cycle, the erythrocytic cycle and transmission process. Salivary vector-based vaccine has the potential to be developed as a malaria vaccine because it can prevent transmission process and also decrease the morbidity of the disease. Saliva from Anopheles contains vasomodulator and immunomodulatory components, that are required in the blood feeding process, but in the same time it could enhance the transmission of the malaria parasite. If the component in the salivary vector can increase pathogen infection, then vaccinating the host with its anti-substances can control the transmission of pathogens (Transmision Blocking Vaccine). Anopheles sundaicus is an important vector of malaria in coastal areas of Java, Bali, Sumatra, Kalimantan and West Nusa Tenggara islands. Repeated exposures of Salivary Gland Extract (SGE) from this vector have been proven to be able to decrease parasitemic rates in mouse model for malaria in our study. The objective of this research is to determine and localize the immunogenic protein from SGE of An. sundaicus as the first step for the characterization of its immunomodulatory component. Mosquito salivary gland protein profile of An.sundaicus was determine by SDS-PAGE. Determination of salivary glands immunogenic proteins was conducted by Western Blotting with IgG from people living from endemic area as primary antibody. Out of 15 bands appeared in SDS PAGE ranging from 24 kD to 138 kD, only two protein bands with molecular weights of 68 and 37 kDa were the most immunogenic. Those immunogenic proteins were consistent recognized by pooled serum of people as well as by individual response. Keywords: malaria, saliva, vector, immunogenic protein, vaccine

Specific sequence of Plasmodium falciparum DBL domains associated with severe malaria outcome Erma Sulistyaningsih; Loeki Enggar Fitri; Thomas Loescher; Nicole Berens-Riha
UNEJ e-Proceeding Indonesian Protein Society (IPS), International Seminar and Workshop 2014
Publisher : UPT Penerbitan Universitas Jember

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Duffy-binding like (DBL) domains of Plasmodium falciparum are believed to be involved in erythrocytes invasion and infected erythrocytes cytoadhesion during the blood stage of malaria infection. In Plasmodium falciparum, DBL domains found in the two different protein families; Erythrocyte Binding Ligand (EBL) including EBA-175, EBA-140, EBA-181 and EBL-1, and Plasmodium falciparum Erythrocyte Membrane Protein-1. The study aimed at investigating the specific sequence of Plasmodium falciparum involved in severe malaria outcome.Blood samples from severe and uncomplicated falciparum malaria cases from Papua and South Kalimantan province, Indonesia, were collected for DNA extraction. A dried blood on filter paper were used for RNA extraction. PCR was performed using UNIEBP primers and directly sequenced. Internal var D primers were designed according to the sequencing of the ~550 bp band produced by UNIEBP primers. The nucleotide sequences were analyzed by NCBI BLAST. Multiple bands ranging from nearly 250 bp to 1 kb were resulted from gDNA in all samples. Two isolates yielded bands of 450 and 525 bp, three isolates showed three bands additionally 250 bp, one isolate presented four bands additionally 800 bp and one isolate resulted one band additionally 1 kb.Amplification of cDNA from severe malaria cases produced one to four bands ranging from 250 bp to 700 bp, and no band observed from cDNA of uncomplicated malaria. Sequencing of the 418 bp bands matched with the eba-175 gene, the 316 bp determined as DBL1a domain and 486 bp band matched with the DBLg domain isolated from placenta of PAM’s Malawian woman. The expression of a 237 bp sequence corresponding to var D gene, was detected solely in severe malaria patients, implicating an association of gene expression and manifestation of severe malaria. Further characterization of the var D gene with a larger sample size is required to draw a definite conclusion. Keywords: DBL domains, Plasmodium falciparum, severe malaria, var D gene.

Malaria Kongenital di Daerah Endemis Indonesia: Studi di RSUD Dr. Tc Hillers Maumere Flores Mario B. Nara; Irene Ratridewi Huwae; Loeki Enggar Fitri; Natalia Erica Jahja
Sari Pediatri Vol 17, No 1 (2015)
Publisher : Badan Penerbit Ikatan Dokter Anak Indonesia (BP-IDAI)

Latar belakang. Di distrik Sumba Barat pada tahun 2004 dilaporkan malaria merupakan penyakit terbanyak. Era transportasi yangtinggi menyebabkan kemungkinan kejadian malaria kongenital di Lembata dan Flores (Maumere) juga tinggiTujuan. Memberikan gambaran mengenai malaria kongenital di RSUD dr. TC. Hillers, Maumere.Metode: Penelitian deskriptif dilakukan mulai Desember 2012 â€“ Desember 2013. Spesimen darah diambil dari neonatus dan ibunya,dikirim dengan dry ice ke Fakultas Kedokteran Universitas Brawijaya dan dilakukan pemeriksaan hapusan darah dan nested PCR.Hasil. Angka kejadian malaria kongenital di RSUD dr. TC. Hillers Maumere selama 1 tahun penelitian 7,78%. Dari 39 subjekyang terinfeksi malaria kongenital, 74,4% terinfeksi P. vivax. Gejala neonatus yang terinfeksi antara lain, anemia (46,2%), sepsis like(28,2%), prematur (38,5%), ikterus (5,5%), dan asimtomatis (48,7%).Kesimpulan. Angka kejadian malaria kongenital di RSUD dr. TC. Hillers Maumere cukup tinggi dan dapat memberikan manifestasiklinis pada bayi yang dilahirkan.

The Effect of C680T GPR43 Gene Variations to Its Interaction with Short Chain Fatty Acid (SCFA) In Type 2 Diabetes Mellitus Rizky Amalia; Karyono Mintaroem; Loeki Enggar Fitri; Nashi Widodo; Hidayat Sujuti
Research Journal of Life Science Vol 6, No 1 (2019)
Publisher : Lembaga Penelitian dan Pengabdian kepada Masyarakat, Universitas Brawijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.21776/ub.rjls.2019.006.01.6

Diabetes is a disorder in the metabolism of carbohydrates, lipids and proteins with various causes. From the previous research, GPR43 is a potent clinical target for the treatment of type 2 diabetes. It can be activated by Short Chain Fatty Acid (SCFA) which is an organic fatty acid produced through fermentation of dietary fiber by bacteria in the distal intestine. The aim of this study was to analyze the effect of C680T GPR43 Gene Variations to Its Interaction with Short Chain Fatty Acid (SCFA) in silico. The study used 8 sequences of GPR43: ID AF024690, AC002511, EU432114, BC095535, BC096198, BC096199, BC096200, BC096201 and data of ligand (SCFA): acetic acid (CID 176), Butyric acid (CID 264) and Propionic acid (CID 1032). GPR43 was modelled using I-TASSER, Sequence and structural alignments were conducted using Bioedit and Superpose V.10, respectively. The Docking process was done using PyRx and molecular interaction was analyzed using Discovery Studio 2016. The Result showed that three types of SCFA bind to GPR43 variants T and GPR43 variant M obtained a similar pattern. The binding affinity from the largest to the smallest is butyric acid > propionic acid > acetic acid. GPR43 variant T has greater affinity to the SCFA than the GPR43 variant M. There is no differences of preference between GPR43 variant T and GPR43 variant M to bind SCFA.

Humoral Response to Anopheles maculatus and Anopheles sundaicus Salivary Gland Proteins Yunita Armiyanti; Widodo widodo; Loeki Enggar Fitri; Teguh Wahju Sardjono
Journal of Agromedicine and Medical Sciences Vol 3 No 2 (2017)
Publisher : Faculty of Medicine, University of Jember

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.19184/ams.v3i2.5071

The salivary gland of female Anopheles mosquito has important role in malaria transmission by salivary proteins that enhancing Plasmodium transmission. The mosquito saliva contains vasomodulatory and immunomodulatory components that inhibit the physiological response of the host. Therefore, the pathogen infects the host without any resistance. The salivary proteins also induce the production of antibody IgG in the host after exposed by the Anopheles mosquito bites repeatedly. This study aims to measured the antibody response of inhabitants living in malaria endemic areas (Kalirejo viilages, Kokap, Kulonprogo) to salivary gland proteins of An. maculatus and An.sundaicus. The level of antibody response was measured by ELISA and analyzed with T test or Anova test for normal distribution of data and Mann Whitney test or Kruskal Wallis test for the data were not normally distributed. The result showed that the level of anti-salivary gland homogenate IgG from sera of people living in malaria endemic area was significantly higher than people living in non-malaria endemic area and negative control (p<0.05). Sera from inhabitants living in Kalirejo village showed that the level of antibody response to both salivary gland homogenate of An.sundaicus and An.maculatus were not significantly different (p<0.05). It was concluded that exposure to An.maculatus and An.sundaicus bites repeatedly could trigger the production of anti-salivary gland proteins IgG antibodies that recognized antigenic proteins from the salivary glands.

Hyperbaric Oxygen Exposure Reduces ICAM-1 And HIF1? Expression in Brain Endothelial Cells from Experimental Cerebral Malaria Mice Prawesty Diah Utami1 , Usman Hadi2 , Yoes Prijatna Dachlan3 , Guritno Suryokusumo4 , Loeki Enggar Fi
Indian Journal of Forensic Medicine & Toxicology Vol. 14 No. 4 (2020): Indian Journal of Forensic Medicine & Toxicology
Publisher : Institute of Medico-legal Publications Pvt Ltd

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.37506/ijfmt.v14i4.12141

This study aimed to reveal the role of ICAM-1 and HIF-1? in brain endothelial cell of cerebral malariamice model after exposure to 2.4 absolute atmospheres (ATA) hyperbaric oxygen (HBO). Thirty-nineC57BL/6 mice were divided into three groups: control negative (normal mice without any exposure),control positive (Plasmodium berghei ANKA [PbA] infection without HBO exposure), and treatment (PbAinfection and exposed to HBO for 10 sessions after the parasite grew). Parasitemia and clinical symptomswere observed every day. Brain tissues were isolated on day 13 post-infection for histopathological andimmunohistochemical examination (observed at 400x magnification in 10 visual fields). HBO decreasedHIF-1? and ICAM-1 expression in endothelial cells. There was a moderate correlation between HIF-1? andICAM-1 expression. Ten HBO sessions prevented cerebral malaria, as denoted by the decreased expressionof ICAM-1 and HIF-1? in brain vascular endothelial cells from the experimental mice.

Induction of Plasmodium falciparum strain 2300 dormant forms by artemisinin Lilik Maslachah; Yoes Prijatna Dachlan; Chairul A. Nidom; Loeki Enggar Fitri
Universa Medicina Vol. 34 No. 1 (2015)
Publisher : Faculty of Medicine, Universitas Trisakti

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.18051/UnivMed.2015.v34.25-34

BACKGROUND The presence of Plasmodium falciparum resistance and decreased efficacy of artemisinin and its derivatives has resulted in the issue of malaria becoming increasingly complex, because there have been no new drugs as artemisinin replacements. The aims of this research were to evaluate in vitro changes in ultrastructural morphology of P. falciparum 2300 strain after exposure to artemisinin. METHODS The research used an experimental design with post test only control group. Cultures of P. falciparum 2300 strain in one control and one mutant group were treated by exposure to artemisinin at IC50 10-7 M for 48 hours. Ultrastructural phenotypic examination of ring, trophozoite and schizont morphology and developmental stage in the control and mutant group were done at 0, 12, 24, 36, 48 hours by making thin blood smears stained with 20% Giemsa for 20 minutes and examined using a microscope light at 1000x magnification. RESULTS Dormant forms occurred after 48 hours of incubation with IC50 10-7 M artemisinin in the control group. In the mutant group, dormant forms, trophozoites with blue cytoplasm and normal schizont developmental stages were seen. Ultrastructural phenotypic morphology at 0, 12, 24, 36, 48 hours showed that in the control group dormant formation already occurred with exposure to IC50 10-7 M, while in the mutant group dormant formation occurred only with exposure to IC50 2.5x10-5 M. CONCLUSION Exposure to artemisinin antimalarials in vitro can cause phenotypic morphological changes of dormancy in P. falciparum Papua 2300 strain.

Toll Like Receptor 4 (Tlr4) And p65 Nuclear Factor Kappa B (Nf-Kb) Expression In Monocyte Cell Of Children With Steroid Resistant Nephrotic Syndrome Tikto Wahyono; Krisni Subandiyah; Loeki Enggar Fitri; Agustina Tri Endharti
Journal of Tropical Life Science Vol. 4 No. 2 (2014)
Publisher : Journal of Tropical Life Science

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This study aimed to prove the difference of TLR4 and subunit p65NF-kB expression between children with steroid-sensitive nephrotic syndrome (SSNS) and those with steroid-resistant nephrotic syndrome (SRNS) and to find out the correlation between expression of TLR4 and p65NF-kB on children with SRNS. Twenty three patients of idiopathic nephrotic syndrome patients (INS) were enrolled in this study and classified into two groupsâ€”those with SSNS (11 patients) and SRNS (12 patients). Peripheral Blood Mononuclear Cells (PBMC) isolation was performed, taken from 5 ml patients blood samples, followed by monocyte isolation of PMBC using monocyte culture. Examination of TLR4 and p65 NF-kB expression from monocyte's cells culture was performed using flow cytometry. All data were processed using Statistical Package for the Social Sciences (SPSS 15) for Windows. From 11 patients that were classified into SSNS group, 81.8% having good nutritional status and 18.2% comprising undernourished status compared to 12 patients of the SRNS group, in which 6 accounting for 41.7% having good nutritional status, 50% having undernourished status and 8.3% having malnourishment status. The average age is 7.59 ± 3.52 and six years old is the highest age studied. Based on normality tests using Shapiro-Wilk, variables of TLR4 have p value of 0.620 and p65 NF-kB have p value of 0.027, showing that the data of TLR4 was distributed normally but p65 NF-kB data was not distributed normally. The test on TLR4 data variation using Levene Test showed its significance value of p was 0.318, meaning that the data was homogeneous. Using unpaired t-test, the differences of TLR4 expression between SSNS and SRNS was significant (p=0.012), while using Mann-Whitney test, the differences of p65 NF-kB expression between SSNS and SRNS showed an insignificant correlation (p=0.880). Pearson correlation test between the expression of TLR4 and p65 NF-kB showed no significant correlation (p=0.472), while Spearman correlation test to see the relationship between expression of TLR4 and SRNS produced correlation value of 0.512 and its importance p value was 0.013 (p

Co-Authors A.A. Ketut Agung Cahyawan W AA Sudharmawan, AA Adilah Ulfiati Adilah Ulfiati, Adilah Agustin Iskandar Agustina Tri Endharti Agustina Tri Endharti Ahmad Fauziansyah Zian Ajeng Maharani Putri Alfian Wika Cahyono Ali Rahmanto Anak Agung Gede Sugianthara Andi Arahmadani Arasy Anik Widijanti Arasy, Andi Arahmadani Ardhian Wardana Ardhian Wardana, Ardhian Ariel, Dio Giovanni Arif Setyawan, Sang Aji Arifin, Mochammad Samsul Astutik Pudjirahaju Bagus Hermansyah BR. Sijabat, Melda Fio Flora Bramantyo Aji Wicaksono Bramantyo Aji Wicaksono, Bramantyo Aji Brigitta Ida RV Corebima Burhan, Niniek Cahyono, Alfian Wika Chairul A. Nidom Chairul A. Nidom Dalhar, Mochamad Damayanti, Ria Dara Dasawulansari Syamsuri Desy Andari Dewi Indiastari Didi Candradikusuma Didi Candradikusuma Dio Giovanni Ariel Dorta Simamora Edi Widjajanto Elviliana, Elviliana Erma Sulistyaningsih Erwan, Nabila Erina Eviana Norahmawati Firdiani Nur Afifah, Firdiani Nur Fitria Febriliani Putri Fitriana Nugraheni Fitriana Nugraheni, Fitriana Ghofar, Hervin Febrina Handono Kalim Hayu Sukowati Nopitasari Heri Kristianto Heri Suroso, Heri Herpan Syafii Harahap Hervin Febrina Ghofar Hidayat Sujuti Husnul Asariati Husnul Asariati I Ketut Gede Muliartha Ihwan Ihwan Ika Setyo Rini Irene Ratridewi Isnadiyah Juhdi Joko Agus Gunawan Josef Sem Berth Tuda Juhdi, Isnadiyah Kana Mardhiyyah Kartika Senjarini Karyono Mintaroem Karyono Mintaroem Karyono Mintaroem Khadafi Indrawan Khairiyadi Khairiyadi Krisni Subandiyah Krisni Subandiyah Krisni Subandiyah Krsni Subandiyah Kusworini Handono Laksmi Karunia Tanuwijaya Laksmi Karunia Tanuwijaya Lilik Maslachah Lilik Zuhriyah M. Fahrul Arifin Mardhiyyah, Kana Mario B. Nara Melda Fio Flora BR. Sijabat Merici, Angela Mochammad Dalhar Moh Mirza Nuryady Moh Mirza Nuryady, Moh Mirza Mohammad Saifur Rahman Mulyohadi Ali Muti'ah, Roihatul Nabila Erina Erwan Nafi’ah, Riris Waladatun Namira, Anggi Alya Nashi Widodo Natalia Erica Jahja Nicole Berens-Riha Nicole Berens-Riha, Nicole Niniek Budiarti B Niniek Burhan Noer Aini Nopitasari, Hayu Sukowati Nugraha, Rivo Yudhinata Brian Nur Fahma Pradiptasari Nur Fahma Pradiptasari, Nur Fahma Nur Hidayat Nur Permatasari Nurdiana Nurdiana Nurdiana Nurdiana Nurtyas, Yunika pertiwi, resti anggun Poedji Hastutiek Pratama, Andhika Putra Agus putra, prasaundra triantoni Putri, Ajeng Maharani Putri, Fitria Febriliani Putri, Rachmania Rachmania Putri Rahma, Zainabur Rahmad Rahmad Rahman, Mohammad Saifur Renny Suwarniaty Renny Suwarniaty, Renny Rifa'i, Muhaimin Rivo Yudhinata Brian Nugraha Rizky Amalia Rohma, Novita Ainur Sabrina Sunyoto, Nimas Mayang Saiful Akhyar Lubis Sakunda Anggarini, Sakunda Samsul Arifin Siti Candra Windu Baktiyani Siti Candra Windu Baktiyani Soebaktiningsih Soebaktiningsih Soemarko Soemarko Sofia, Ovi Sri Hayati, Yati Sri Murwani Sri Poeranto, Sri Sri Suhartini Sri Winarsih Subekti, Indah Fitriana Sudjari Sudjari Sugeng Setyo Utomo Sugeng Setyo Utomo, Sugeng Setyo Sujarot Dwi Sasmito sujarot dwi sasmito, sujarot dwi Sumarno . Susanto Nugroho Susanto Nugroho Sutiman B. Sumitro Swastomo, Rahadi Syarkiah Syarkiah Teguh Wahju Sardjono Teguh Wahju Sardjono Teguh Wahju Sardjono Thomas Loescher Thomas Loescher, Thomas Tikto Wahyono Tinny Endang Endang H Tinny Endang Hernowati Tinny Endang Hernowati Tuda, Josef Sem Berth Umar Zein Verry Asfirizal Vonny Mariany Deckert Wahyono, Tikto Wongso Suhendro Yoes Prijatna Dachlan Yuanita Mulyastuti Yuliyanik yuliyanik Yunika Nurtyas Yunita Armiyanti Zainabur Rahma Zakiyah Zulaifa Zakiyah Zulaifa, Zakiyah

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