Filariasis is a as Filarioidea infection caused by parasitic (roundworms) spread by different Disease vector. They are included in the list of neglected tropical diseases.
The most common type is lymphatic filariasis caused by three species of Filaria that are spread by mosquitoes. Other types of filariasis are onchocerciasis also known as river blindness caused by Onchocerca volvulus; Loa loa filariasis (Loiasis) caused by Loa loa; Mansonelliasis caused by three species of Mansonella, and Dirofilariasis caused by two types of Dirofilaria. All of these worms belong to the superfamily Filarioidea.
These worms are transmitted by infected mosquitoes of the genera Aedes, Culex, Anopheles and Mansonia.
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Individuals infected by filarial worms may be described as either "microfilaraemic" or "amicrofilaraemic", depending on whether microfilariae can be found in their peripheral blood. Filariasis is diagnosed in microfilaraemic cases primarily through direct observation of microfilariae in the peripheral blood.
Cases of acute inflammatory filariasis manifest 5 to 7 day episodes of fever along with inflammation of lymph nodes. It is often accompanied by epididymitis and spermatic cord inflammation. Secondary bacterial infections are very common and are seen to be more severe in previously unexposed immigrants than in native residents. Chronic filarial disease develops gradually over the years. In most patients the lymphatic dilation does not present any physical symptoms. However, inflammatory responses to dying adult worms often lead to chronic lymphedema in the affected regions which then progresses to elephantiasis. W. bancrofti often causes hydrocele and scrotal elephantiasis. Moreover, disruption of lymphatic vessels or aberrant drainage of lymph fluid often leads to chyluria and chyloceles.( Red Book: 2021–2024 Report of the Committee on Infectious Diseases, Lymphatic Filariasis (Bancroftian, Malayan, and Timorian), 2021
Elephantiasis affects mainly the lower extremities, while the , , and amputation stumps are affected less frequently. However, different species of filarial worms tend to affect different parts of the body; Wuchereria bancrofti can affect the legs, arms, vulva, breasts, and scrotum (causing hydrocele formation), while Brugia timori rarely affects the genitals. Those who develop the chronic stages of elephantiasis are usually free from microfilariae (amicrofilaraemic), and often have adverse immunological reactions to the microfilariae, as well as the adult worms.
The subcutaneous worms present with rashes, urticarial , and arthritis, as well as hyper- and hypopigmentation . Onchocerca volvulus manifests itself in the eyes, causing "river blindness" (onchocerciasis), one of the leading causes of blindness in the world. Serous cavity filariasis presents with symptoms similar to subcutaneous filariasis, in addition to abdominal pain, because these worms are also deep-tissue dwellers.
In past, one of the first successes in the efforts to improve sensitivity and specificity of filarial diagnostic tests was identification of the repeated sequences in the parasite genome. The advancement in technologies like polymerase chain reaction (PCR) led to the development of various assays that made large scale surveys of parasitic prevalence much easier.Pastor, A. F., Silva, M. R., dos Santos, W. J. T., Rego, T., Brandão, E., de-Melo, Neto, O. P., & Rocha, A. (2021). Recombinant antigens used as diagnostic tools for lymphatic filariasis. Parasites & Vectors, 14(1), 474. https://doi.org/10.1186/s13071-021-04980-3
Filarial parasites are known to induce several immunoregulatory mechanisms like the activation of macrophages and T regulatory cells. It has been found that T regulatory cells play an essential role in how filarial worms modify the host immune response by producing immunoglobulin G4 (IgG4). A very high plasma content of IgG4 has been recorded in asymptomatic patients of LF. Thus, the newer assays measuring IgG4 responses to crude filarial extracts or using fractions of parasite extracts have a better overall specificity but are not efficient in discriminating microfilaremic from amicrofilaremic serum donors. Assays which measure circulating antigen are expected to be better at measuring active infection because only living worms secrete circulating antigen.Harnett, W., Bradley, J. E., & Garate, T. (1998). Molecular and immunodiagnosis of human filarial nematode infections. Parasitology, 117 Suppl, S59-71. https://doi.org/10.1017/s0031182099004084
As an attempt to come up with immunodiagnostic test kits for detection of circulating filarial antigen, numerous Antigens and Antibodies specific to the parasites have been tested. An Og4C3 monoclonal antibody-based ELISA and an immunochromatographic ( ICT) card test using the same monoclonal antibody have been tested. However, these commercial assays have certain issues with respect to stability, cost and specificity in field applications. Moreover, it was seen that the ICT format showed 25% of microfilarial negative individuals as being positive for circulating filarial antigens.Janardhan, S., Pandiaraja, P., Pandey, V., Karande, A., & Kaliraj, P. (2011).
Development and characterization of monoclonal antibodies against WbSXP-1 for
These commercial tests based on the above circulating antigens are also limited to
successful detection of only adult bancroftian worms, making diagnosis only possible in later stages of infection when the therapeutics might no more show effect. A search for worm specific antigens was initiated where SXP-1 antigen was recognized to be specific for W.bancrofti filariasis. The antigen was identified after screening the cDNA library of adult worms with serum from both amicrofilaremic and microfilaremic patients.The native SXP-1 antigen was present in extracts of microfilariae and adult worms and were seen to be not specific to any lifecycle stage.Dissanayake, S., Xu, M., & Piessens, W. F. (1992). A cloned antigen for serological diagnosis of Wuchereria bancrofti microfilaremia with daytime blood samples. Molecular and Biochemical Parasitology, 56(2), 269–277.
https://doi.org/10.1016/0166-6851(92)90176-k
To identify a W. bancrofti-specific antigen, pastor et al., used the Bm SXP gene to screen against the W.bancrofti Larval stage 3 cDNA library. This led to the identification of a cDNA sequence of W.bancrofti SXP-1 that encoded for a polypeptide with a predicted molecular weight of 20.8 kDa. Wb-SXP was found to be 85 percent identical to the BmSXP polypeptide and differed along the C terminal where the former had an extra 29 amino acid long extension. The WbSXP-1 variant, where a stop codon has been introduced at the amino acid position 153 has been shown to be widely distributed among different W.bancrofti populations. Searches carried out with available sequences from various worms revealed the presence of SXP-1 homologs in many other nematodes with substantial identities in sequence observed during pairwise comparisons. Some examples include O.volvulus (50% identity; Ov-SXP-1), Ascaris suum (43%; As-SXP-1), Loa loa (46%; Li-SXP-1), and C.elegans (29%; Ce-SXP-1).The presence of a number of invariant and conserved residues in all of these nematode-derived molecules suggests that Wb-SXP-1 is a member of a new protein family.Rao, K. V., Eswaran, M., Ravi, V., Gnanasekhar, B., Narayanan, R. B., Kaliraj,
P., Jayaraman, K., Marson, A., Raghavan, N., & Scott, A. L. (2000). The
Wuchereria bancrofti orthologue of Brugia malayi SXP1 and the diagnosis of
bancroftian filariasis. Molecular and Biochemical Parasitology, 107(1), 71–80.
https://doi.org/10.1016/s0166-6851(99)00231-5
Different trials were made to use the known drug at its maximum capacity in absence of new drugs. In a study from India, it was shown that a formulation of albendazole had better anti-filarial efficacy than albendazole itself.
In 2003, the common antibiotic doxycycline was suggested for treating elephantiasis. Filarial parasites have symbiotic bacteria in the genus Wolbachia, which live inside the worm and seem to play a major role in both its reproduction and the development of the disease. This drug has shown signs of inhibiting the reproduction of the bacteria, further inducing sterility in the nematode.
Clinical trials in June 2005 by the Liverpool School of Tropical Medicine reported an eight-week course almost eliminated microfilaraemia.
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Treatment
Society and culture
Research teams
Prospects for elimination
Other animals
Cattle
Horses
Dogs
See also
Further reading
External links
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